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Bibliography: leaves 209-254. / xv, 254 leaves : ill. (chiefly col.) ; 30 cm. / Title page, contents and abstract only. The complete thesis in print form is available from the University Library. / Experiments detailed in this thesis, evaluate the impact of various herbicides and herbicide mixtures on the growth, nodulation and nitrogen fixation of annual pasture legumes, the efficacy of the herbicides for weed control, and the potential role of mechanical defoliation to replace herbicides, leading to lower cost and more sustainable farming systems. / Thesis (Ph.D.)--University of Adelaide, Dept. of Plant Science, 1996

Legume-rhizobia symbioses contribute at least 20% of the biosphere's supply of reactive nitrogen. These unique associations rely on the exchange of specific molecular signals between nitrogen-fixing soil bacteria, collectively called rhizobia, and their host plants and, with few exceptions, result in the formation of root nodules, which provide an environment suitable for nitrogen fixation. However, nitrogen fixation is energetically expensive and nodule proliferation, in much the same manner as the proliferation of other meristems in plants, must be controlled in order to attain equilibrium between cell proliferation and differentiation. Nodule proliferation is controlled primarily and systemically by autoregulation of nodulation (AON). A gene central to this process was first isolated by map-based cloning from soybean (Glycine max) and was named G. max Nodule Autoregulation Receptor Kinase (GmNARK) in accordance with its biochemical and physiological functions. Expression patterns of GmNARK have been described by several investigators; however, these reports were based on either non-quantitative methods or a limited number of tissue types. More importantly, the expression domains of GmNARK were completely unknown. The study described in this thesis utilised techniques such as quantitative RT-PCR (QRTPCR), transcription start site mapping, promoter-reporter gene fusion, and promoter deletion, to analyse the expression levels and domains of GmNARK across a variety of tissues as well as identify the promoter elements that are responsible for the basal and tissue-specific expression of GmNARK. In addition, the promoter activity of GmNARK was also compared with that of Lotus japonicus HAR1, the GmNARK orthologue, in both homologous and heterologous transformation systems. Based on QRT-PCR, GmNARK was expressed to varying levels throughout the plant; the transcript was detected at high levels in mature leaves and roots but to a lesser extent in young leaves, shoot tips and nodules. The transcript level was not significantly affected by Bradyrhizobium japonicum during the first week following inoculation. Histochemical analysis of L. japonicus plants carrying either a 1.7 kb GmNARK promoter or 2.0 kb LjHAR1 promoter fused to a beta-glucuronidase reporter gene localised GUS activity to living cells within vascular bundles, especially phloem cells in leaves, stems, roots, and nodules. Phloem-specific expression was also detected in soybean hairy roots carrying these constructs. These results suggested that both cis- and trans-acting elements required for the transcriptional regulation of these orthologous genes are likely to be conserved. In contrast, 1.7 kb of the GmNARK promoter did not drive phloem-specific expression in Arabidopsis thaliana, indicating the absence of the trans-acting elements required for the tissue-specificity of GmNARK in this distantly related species. The comparison of 2.0 kb of promoter sequences of GmNARK, LjHAR1 and Medicago truncatula SUNN, another GmNARK orthologue, using bioinformatics and computational approaches indicated several highly conserved motifs including a putative negative regulatory region (NRR), which was previously reported to repress gene expression in non-phloem cell types. Deletion analysis of the GmNARK promoter, however, ruled out the possibility that this motif, found at -308 bp with respect to the translation start site, was truly functional and located the region controlling phloem-specific expression to DNA sequence between 908 bp and 1.7 kb upstream of the start codon. Two other candidate regions were identified by Multiple EM for Motif Elicitation (MEME). These regions, namely MEME3 and MEME4 showed strong sequence similarity to the corresponding regions of the LjHAR1 promoter. Interestingly, the MEME3 motif was also found in the MtSUNN promoter at a similar location to that of LjHAR1. Potential NRRs in the LjHAR1 and MtSUNN promoters were found in the MEME3 motifs, whereas only a variant form of a NRR in the GmNARK promoter was found in this region. Additionally, an identical semi-palindromic sequence was also observed in the MEME3 motifs of the three orthologous promoters. Based on these findings, the semi-palindromic sequence and the variant form of the NRR are proposed to be positive and negative regulatory elements for the phloem-specific expression of GmNARK, respectively. The computational approaches also identified two potential TATA elements in the GmNARK promoter. Rapid amplification of 5' cDNA ends and promoter deletion analysis have confirmed that they were functional. The two TATA elements in GmNARK promoter appeared to cooperatively direct transcription of GmNARK, but either was adequate for basal transcription. The finding that the expression of AON receptor-like kinase genes is phloem-specific has contributed to a better understanding of AON signalling pathways. The QRT-PCR study and the discovery of cis-acting regulatory regions have also provided crucial information on the transcriptional regulation of GmNARK as well as plant genes in general. Additionally, the promoters of GmNARK and LjHAR1 could potentially be used to drive phloem-specific expression in legume biotechnology research.

Legume-rhizobia symbioses contribute at least 20% of the biosphere's supply of reactive nitrogen. These unique associations rely on the exchange of specific molecular signals between nitrogen-fixing soil bacteria, collectively called rhizobia, and their host plants and, with few exceptions, result in the formation of root nodules, which provide an environment suitable for nitrogen fixation. However, nitrogen fixation is energetically expensive and nodule proliferation, in much the same manner as the proliferation of other meristems in plants, must be controlled in order to attain equilibrium between cell proliferation and differentiation. Nodule proliferation is controlled primarily and systemically by autoregulation of nodulation (AON). A gene central to this process was first isolated by map-based cloning from soybean (Glycine max) and was named G. max Nodule Autoregulation Receptor Kinase (GmNARK) in accordance with its biochemical and physiological functions. Expression patterns of GmNARK have been described by several investigators; however, these reports were based on either non-quantitative methods or a limited number of tissue types. More importantly, the expression domains of GmNARK were completely unknown. The study described in this thesis utilised techniques such as quantitative RT-PCR (QRTPCR), transcription start site mapping, promoter-reporter gene fusion, and promoter deletion, to analyse the expression levels and domains of GmNARK across a variety of tissues as well as identify the promoter elements that are responsible for the basal and tissue-specific expression of GmNARK. In addition, the promoter activity of GmNARK was also compared with that of Lotus japonicus HAR1, the GmNARK orthologue, in both homologous and heterologous transformation systems. Based on QRT-PCR, GmNARK was expressed to varying levels throughout the plant; the transcript was detected at high levels in mature leaves and roots but to a lesser extent in young leaves, shoot tips and nodules. The transcript level was not significantly affected by Bradyrhizobium japonicum during the first week following inoculation. Histochemical analysis of L. japonicus plants carrying either a 1.7 kb GmNARK promoter or 2.0 kb LjHAR1 promoter fused to a beta-glucuronidase reporter gene localised GUS activity to living cells within vascular bundles, especially phloem cells in leaves, stems, roots, and nodules. Phloem-specific expression was also detected in soybean hairy roots carrying these constructs. These results suggested that both cis- and trans-acting elements required for the transcriptional regulation of these orthologous genes are likely to be conserved. In contrast, 1.7 kb of the GmNARK promoter did not drive phloem-specific expression in Arabidopsis thaliana, indicating the absence of the trans-acting elements required for the tissue-specificity of GmNARK in this distantly related species. The comparison of 2.0 kb of promoter sequences of GmNARK, LjHAR1 and Medicago truncatula SUNN, another GmNARK orthologue, using bioinformatics and computational approaches indicated several highly conserved motifs including a putative negative regulatory region (NRR), which was previously reported to repress gene expression in non-phloem cell types. Deletion analysis of the GmNARK promoter, however, ruled out the possibility that this motif, found at -308 bp with respect to the translation start site, was truly functional and located the region controlling phloem-specific expression to DNA sequence between 908 bp and 1.7 kb upstream of the start codon. Two other candidate regions were identified by Multiple EM for Motif Elicitation (MEME). These regions, namely MEME3 and MEME4 showed strong sequence similarity to the corresponding regions of the LjHAR1 promoter. Interestingly, the MEME3 motif was also found in the MtSUNN promoter at a similar location to that of LjHAR1. Potential NRRs in the LjHAR1 and MtSUNN promoters were found in the MEME3 motifs, whereas only a variant form of a NRR in the GmNARK promoter was found in this region. Additionally, an identical semi-palindromic sequence was also observed in the MEME3 motifs of the three orthologous promoters. Based on these findings, the semi-palindromic sequence and the variant form of the NRR are proposed to be positive and negative regulatory elements for the phloem-specific expression of GmNARK, respectively. The computational approaches also identified two potential TATA elements in the GmNARK promoter. Rapid amplification of 5' cDNA ends and promoter deletion analysis have confirmed that they were functional. The two TATA elements in GmNARK promoter appeared to cooperatively direct transcription of GmNARK, but either was adequate for basal transcription. The finding that the expression of AON receptor-like kinase genes is phloem-specific has contributed to a better understanding of AON signalling pathways. The QRT-PCR study and the discovery of cis-acting regulatory regions have also provided crucial information on the transcriptional regulation of GmNARK as well as plant genes in general. Additionally, the promoters of GmNARK and LjHAR1 could potentially be used to drive phloem-specific expression in legume biotechnology research.

Legume-rhizobia symbioses contribute at least 20% of the biosphere's supply of reactive nitrogen. These unique associations rely on the exchange of specific molecular signals between nitrogen-fixing soil bacteria, collectively called rhizobia, and their host plants and, with few exceptions, result in the formation of root nodules, which provide an environment suitable for nitrogen fixation. However, nitrogen fixation is energetically expensive and nodule proliferation, in much the same manner as the proliferation of other meristems in plants, must be controlled in order to attain equilibrium between cell proliferation and differentiation. Nodule proliferation is controlled primarily and systemically by autoregulation of nodulation (AON). A gene central to this process was first isolated by map-based cloning from soybean (Glycine max) and was named G. max Nodule Autoregulation Receptor Kinase (GmNARK) in accordance with its biochemical and physiological functions. Expression patterns of GmNARK have been described by several investigators; however, these reports were based on either non-quantitative methods or a limited number of tissue types. More importantly, the expression domains of GmNARK were completely unknown. The study described in this thesis utilised techniques such as quantitative RT-PCR (QRTPCR), transcription start site mapping, promoter-reporter gene fusion, and promoter deletion, to analyse the expression levels and domains of GmNARK across a variety of tissues as well as identify the promoter elements that are responsible for the basal and tissue-specific expression of GmNARK. In addition, the promoter activity of GmNARK was also compared with that of Lotus japonicus HAR1, the GmNARK orthologue, in both homologous and heterologous transformation systems. Based on QRT-PCR, GmNARK was expressed to varying levels throughout the plant; the transcript was detected at high levels in mature leaves and roots but to a lesser extent in young leaves, shoot tips and nodules. The transcript level was not significantly affected by Bradyrhizobium japonicum during the first week following inoculation. Histochemical analysis of L. japonicus plants carrying either a 1.7 kb GmNARK promoter or 2.0 kb LjHAR1 promoter fused to a beta-glucuronidase reporter gene localised GUS activity to living cells within vascular bundles, especially phloem cells in leaves, stems, roots, and nodules. Phloem-specific expression was also detected in soybean hairy roots carrying these constructs. These results suggested that both cis- and trans-acting elements required for the transcriptional regulation of these orthologous genes are likely to be conserved. In contrast, 1.7 kb of the GmNARK promoter did not drive phloem-specific expression in Arabidopsis thaliana, indicating the absence of the trans-acting elements required for the tissue-specificity of GmNARK in this distantly related species. The comparison of 2.0 kb of promoter sequences of GmNARK, LjHAR1 and Medicago truncatula SUNN, another GmNARK orthologue, using bioinformatics and computational approaches indicated several highly conserved motifs including a putative negative regulatory region (NRR), which was previously reported to repress gene expression in non-phloem cell types. Deletion analysis of the GmNARK promoter, however, ruled out the possibility that this motif, found at -308 bp with respect to the translation start site, was truly functional and located the region controlling phloem-specific expression to DNA sequence between 908 bp and 1.7 kb upstream of the start codon. Two other candidate regions were identified by Multiple EM for Motif Elicitation (MEME). These regions, namely MEME3 and MEME4 showed strong sequence similarity to the corresponding regions of the LjHAR1 promoter. Interestingly, the MEME3 motif was also found in the MtSUNN promoter at a similar location to that of LjHAR1. Potential NRRs in the LjHAR1 and MtSUNN promoters were found in the MEME3 motifs, whereas only a variant form of a NRR in the GmNARK promoter was found in this region. Additionally, an identical semi-palindromic sequence was also observed in the MEME3 motifs of the three orthologous promoters. Based on these findings, the semi-palindromic sequence and the variant form of the NRR are proposed to be positive and negative regulatory elements for the phloem-specific expression of GmNARK, respectively. The computational approaches also identified two potential TATA elements in the GmNARK promoter. Rapid amplification of 5' cDNA ends and promoter deletion analysis have confirmed that they were functional. The two TATA elements in GmNARK promoter appeared to cooperatively direct transcription of GmNARK, but either was adequate for basal transcription. The finding that the expression of AON receptor-like kinase genes is phloem-specific has contributed to a better understanding of AON signalling pathways. The QRT-PCR study and the discovery of cis-acting regulatory regions have also provided crucial information on the transcriptional regulation of GmNARK as well as plant genes in general. Additionally, the promoters of GmNARK and LjHAR1 could potentially be used to drive phloem-specific expression in legume biotechnology research.

Legume-rhizobia symbioses contribute at least 20% of the biosphere's supply of reactive nitrogen. These unique associations rely on the exchange of specific molecular signals between nitrogen-fixing soil bacteria, collectively called rhizobia, and their host plants and, with few exceptions, result in the formation of root nodules, which provide an environment suitable for nitrogen fixation. However, nitrogen fixation is energetically expensive and nodule proliferation, in much the same manner as the proliferation of other meristems in plants, must be controlled in order to attain equilibrium between cell proliferation and differentiation. Nodule proliferation is controlled primarily and systemically by autoregulation of nodulation (AON). A gene central to this process was first isolated by map-based cloning from soybean (Glycine max) and was named G. max Nodule Autoregulation Receptor Kinase (GmNARK) in accordance with its biochemical and physiological functions. Expression patterns of GmNARK have been described by several investigators; however, these reports were based on either non-quantitative methods or a limited number of tissue types. More importantly, the expression domains of GmNARK were completely unknown. The study described in this thesis utilised techniques such as quantitative RT-PCR (QRTPCR), transcription start site mapping, promoter-reporter gene fusion, and promoter deletion, to analyse the expression levels and domains of GmNARK across a variety of tissues as well as identify the promoter elements that are responsible for the basal and tissue-specific expression of GmNARK. In addition, the promoter activity of GmNARK was also compared with that of Lotus japonicus HAR1, the GmNARK orthologue, in both homologous and heterologous transformation systems. Based on QRT-PCR, GmNARK was expressed to varying levels throughout the plant; the transcript was detected at high levels in mature leaves and roots but to a lesser extent in young leaves, shoot tips and nodules. The transcript level was not significantly affected by Bradyrhizobium japonicum during the first week following inoculation. Histochemical analysis of L. japonicus plants carrying either a 1.7 kb GmNARK promoter or 2.0 kb LjHAR1 promoter fused to a beta-glucuronidase reporter gene localised GUS activity to living cells within vascular bundles, especially phloem cells in leaves, stems, roots, and nodules. Phloem-specific expression was also detected in soybean hairy roots carrying these constructs. These results suggested that both cis- and trans-acting elements required for the transcriptional regulation of these orthologous genes are likely to be conserved. In contrast, 1.7 kb of the GmNARK promoter did not drive phloem-specific expression in Arabidopsis thaliana, indicating the absence of the trans-acting elements required for the tissue-specificity of GmNARK in this distantly related species. The comparison of 2.0 kb of promoter sequences of GmNARK, LjHAR1 and Medicago truncatula SUNN, another GmNARK orthologue, using bioinformatics and computational approaches indicated several highly conserved motifs including a putative negative regulatory region (NRR), which was previously reported to repress gene expression in non-phloem cell types. Deletion analysis of the GmNARK promoter, however, ruled out the possibility that this motif, found at -308 bp with respect to the translation start site, was truly functional and located the region controlling phloem-specific expression to DNA sequence between 908 bp and 1.7 kb upstream of the start codon. Two other candidate regions were identified by Multiple EM for Motif Elicitation (MEME). These regions, namely MEME3 and MEME4 showed strong sequence similarity to the corresponding regions of the LjHAR1 promoter. Interestingly, the MEME3 motif was also found in the MtSUNN promoter at a similar location to that of LjHAR1. Potential NRRs in the LjHAR1 and MtSUNN promoters were found in the MEME3 motifs, whereas only a variant form of a NRR in the GmNARK promoter was found in this region. Additionally, an identical semi-palindromic sequence was also observed in the MEME3 motifs of the three orthologous promoters. Based on these findings, the semi-palindromic sequence and the variant form of the NRR are proposed to be positive and negative regulatory elements for the phloem-specific expression of GmNARK, respectively. The computational approaches also identified two potential TATA elements in the GmNARK promoter. Rapid amplification of 5' cDNA ends and promoter deletion analysis have confirmed that they were functional. The two TATA elements in GmNARK promoter appeared to cooperatively direct transcription of GmNARK, but either was adequate for basal transcription. The finding that the expression of AON receptor-like kinase genes is phloem-specific has contributed to a better understanding of AON signalling pathways. The QRT-PCR study and the discovery of cis-acting regulatory regions have also provided crucial information on the transcriptional regulation of GmNARK as well as plant genes in general. Additionally, the promoters of GmNARK and LjHAR1 could potentially be used to drive phloem-specific expression in legume biotechnology research.

Legume-rhizobia symbioses contribute at least 20% of the biosphere's supply of reactive nitrogen. These unique associations rely on the exchange of specific molecular signals between nitrogen-fixing soil bacteria, collectively called rhizobia, and their host plants and, with few exceptions, result in the formation of root nodules, which provide an environment suitable for nitrogen fixation. However, nitrogen fixation is energetically expensive and nodule proliferation, in much the same manner as the proliferation of other meristems in plants, must be controlled in order to attain equilibrium between cell proliferation and differentiation. Nodule proliferation is controlled primarily and systemically by autoregulation of nodulation (AON). A gene central to this process was first isolated by map-based cloning from soybean (Glycine max) and was named G. max Nodule Autoregulation Receptor Kinase (GmNARK) in accordance with its biochemical and physiological functions. Expression patterns of GmNARK have been described by several investigators; however, these reports were based on either non-quantitative methods or a limited number of tissue types. More importantly, the expression domains of GmNARK were completely unknown. The study described in this thesis utilised techniques such as quantitative RT-PCR (QRTPCR), transcription start site mapping, promoter-reporter gene fusion, and promoter deletion, to analyse the expression levels and domains of GmNARK across a variety of tissues as well as identify the promoter elements that are responsible for the basal and tissue-specific expression of GmNARK. In addition, the promoter activity of GmNARK was also compared with that of Lotus japonicus HAR1, the GmNARK orthologue, in both homologous and heterologous transformation systems. Based on QRT-PCR, GmNARK was expressed to varying levels throughout the plant; the transcript was detected at high levels in mature leaves and roots but to a lesser extent in young leaves, shoot tips and nodules. The transcript level was not significantly affected by Bradyrhizobium japonicum during the first week following inoculation. Histochemical analysis of L. japonicus plants carrying either a 1.7 kb GmNARK promoter or 2.0 kb LjHAR1 promoter fused to a beta-glucuronidase reporter gene localised GUS activity to living cells within vascular bundles, especially phloem cells in leaves, stems, roots, and nodules. Phloem-specific expression was also detected in soybean hairy roots carrying these constructs. These results suggested that both cis- and trans-acting elements required for the transcriptional regulation of these orthologous genes are likely to be conserved. In contrast, 1.7 kb of the GmNARK promoter did not drive phloem-specific expression in Arabidopsis thaliana, indicating the absence of the trans-acting elements required for the tissue-specificity of GmNARK in this distantly related species. The comparison of 2.0 kb of promoter sequences of GmNARK, LjHAR1 and Medicago truncatula SUNN, another GmNARK orthologue, using bioinformatics and computational approaches indicated several highly conserved motifs including a putative negative regulatory region (NRR), which was previously reported to repress gene expression in non-phloem cell types. Deletion analysis of the GmNARK promoter, however, ruled out the possibility that this motif, found at -308 bp with respect to the translation start site, was truly functional and located the region controlling phloem-specific expression to DNA sequence between 908 bp and 1.7 kb upstream of the start codon. Two other candidate regions were identified by Multiple EM for Motif Elicitation (MEME). These regions, namely MEME3 and MEME4 showed strong sequence similarity to the corresponding regions of the LjHAR1 promoter. Interestingly, the MEME3 motif was also found in the MtSUNN promoter at a similar location to that of LjHAR1. Potential NRRs in the LjHAR1 and MtSUNN promoters were found in the MEME3 motifs, whereas only a variant form of a NRR in the GmNARK promoter was found in this region. Additionally, an identical semi-palindromic sequence was also observed in the MEME3 motifs of the three orthologous promoters. Based on these findings, the semi-palindromic sequence and the variant form of the NRR are proposed to be positive and negative regulatory elements for the phloem-specific expression of GmNARK, respectively. The computational approaches also identified two potential TATA elements in the GmNARK promoter. Rapid amplification of 5' cDNA ends and promoter deletion analysis have confirmed that they were functional. The two TATA elements in GmNARK promoter appeared to cooperatively direct transcription of GmNARK, but either was adequate for basal transcription. The finding that the expression of AON receptor-like kinase genes is phloem-specific has contributed to a better understanding of AON signalling pathways. The QRT-PCR study and the discovery of cis-acting regulatory regions have also provided crucial information on the transcriptional regulation of GmNARK as well as plant genes in general. Additionally, the promoters of GmNARK and LjHAR1 could potentially be used to drive phloem-specific expression in legume biotechnology research.

Subterranean clover mottle virus (SCMoV) is a positive sense, single-stranded RNA virus that infects subterranean clover (Trifolium subterraneum) and a number of related legume species. The ultimate aim of this research was to investigate aspects of SCMoV that would support its use as a gene silencing vector for legume species, since RNA (gene) silencing is now a potential tool for studylng gene function. The ability of viruses to induce an antiviral defense system is being explored by virus-induced gene silencing (VIGS), in which engmeered viral genomes are used as vectors to introduce genes or gene ii-agments to understand the function of endogenous genes by silencing them. To develop a gene silencing vector, a number of aspects of SCMoV host range and molecular biology needed to be studied. A requirement for a useful viral vector is a suitably wide host range. Hence the first part of this work involved study of the host range and symptom development of SCMoV in a range of leguminous and non-leguminous plants. The aim of this work was to identify new and most suitable hosts among economically important crop and model legumes for functional genomic studies, and also to study symptom development in these hosts for comparison with host responses to any SCMoV-based viral vectors that might be used in later infection studies. A total of 61 plant genotypes representing 52 species from 25 different genera belonging to 7 families were examined for their response to SCMoV infection, including established and new crop legumes, established pasture, and novel pasture and forage legumes, and 12 host indicator plants belonging to the families Amaranthaceae, Apiaceae, Chenopodiaceae, Cruciferae, Cucurbitaceae and Solanaceae. Following mechanical inoculation, plants were examined for symptoms and tested for primary and secondary infection by RT-PCR andlor ELISA after 2-3 weeks and 3-9 weeks, respectively. Thirty-six legume hosts belonging to eight different genera of legumes were identified as suitable hosts of SCMoV, 22 of them systemic hosts and 15 were infected locally. Only two non-legumes were infected with SCMoV-P23, one systemically and one as a local host, so confirming that SCMoV is essentially a legume-infecting virus. This work considerably expanded knowledge of the host range of SCMoV. To provide the information needed to modify the SCMoV genome to develop gene vectors, the virus was characterized in detail. The complete genomes of four isolates, SCMoV-AL, SCMoV-MB, SCMoV-MJ and SCMoV-pFL, were sequenced using high fidelity RT-PCR and molecular cloning, and compared to the first sequenced isolate (SCMoV-P23) to give a complete picture of the genome organisation of the virus. The 4,258 nucleotide (nt) sequence of SCMoV RNA is not polyadenylated. The 5' non-coding region (NCR) is 68 nt in length and the 3' NCR is 174 nt. The coding regon contains four overlapping open reading fi-ames (ORFs). The first, OW1 (nt 68-608), encodes a putative protein containing 179 amino acids with a calculated molecular mass (Ma,) of 20.3 kDa. It overlaps with the next ORF, ORF2a, by four bases. ORF2a (nt 605-2347) encodes a putative protein of 580 amino acids with a Ma, of 63.7 kDa and contains a motif characteristic of chymotrypsin-like serine proteases. The ORF2b is probably translated as part of a polyprotein by -1 ribosomal fiameshifting in ORF2a. The transfiame product (Ma, = 107.5 kDa) is made up of 966 amino acids. A GDD motif typical of RNA virus polymerases is present in ORF2b. The 3' terminal ORF3 (nt 3323-4084) encodes the 27.3 kDa coat protein (CP). Nucleotide variation between the complete sequences of the isolates was two to three orders of magnitude larger than base misincoporation rates of the polymerases used in RT-PCR. Molecular relationship analysis between all five isolates, undertaken with the complete nucleotide sequences, clearly separated them into three groups. These groups reflect similar significantly diverse groupings based on the symptoms and their severity in subterranean clover. Intra-isolate sequence variability is therefore a possible cause of the differences in symptom severity. The analysis also showed that there were more nucleotide substitutions at the 5' terminal half of SCMoV than at the 3' end. This observation was confirmed by the higher value of nucleotide diversities at nonsynonymous versus synonymous sites (dN/ds ratio) estimated for the ORF1, compared to the near conservation of sequences of the other ORFs. These results, together with functional and comparative sequence analysis with other sobemoviruses, implicate the ORFl gene product in pathogenicity of SCMoV, possibly as a severity determinant or as a viral suppressor of RNA silencing in plants. Because more information on SCMoV genome function was required, the possible involvement of the ORFl gene product (PI) and the CP in movement of SCMoV was studied in cells of grasspea (Lathyrus clymenum L) and chickpea as C-terminal fusion constructs with jellyfish (Aequorea victoriae) green fluorescent protein (GFP). A transient expression vector, pTEV, for in planta synthesis of reporter gene constructs was developed. The vector was based on pGEM-T with 35s RNA transcriptional promoter of Caulzjlower Mosaic virus (CaMV) and nopaline synthase gene transcription terminator signal (T-Nos) separated by a multiple subcloning site. A custom-made particle inflow gun was used to introduce the constructs into plant cells. The bombardment conditions were fxst optimised for efficient delivery of DNAcoated particles. Transient gene expression of GFP was monitored 24-96 hours after particle bombardment. Fluorescence from GFP alone, GFP:CP and GFP:Pl constructs was observed in the nucleus of single cells, cytoplasm and cell periphery of neighbouring cells. There was limited spread of these fusion proteins from one cell to another 36-48 hours after transformation. These results indicate that the P 1 and CP cannot move independently from cell to cell. Other viral/cellular components might be needed to form a complex with these proteins to transport the viral genome. Putative nuclear export signals in the P1 and CP sequences of SCMoV were identified by sequence comparison. These could be tested by mutagenesis using full-length infectious clones. To determine the possibility of gene expression of vectors based on SCMoV, three forms of a full-length cDNA clone of SCMoV-pFL were developed: one with no heterologous transcriptional factors (pFL), a second under the control of only 35s (p35SFL) and a third with 35s and T-Nos (pTEVFL). Fifteen day-old in vitro-cultured chickpea, grasspea and subterranean clover seedlings were inoculated by particle bombardment using gold particles coated with plasmid pTEVFL. In vivo-transcribed RNA transcripts were detected by RT-PCR after two weeks in grasspea but not in subterranean clover and chickpea. Experiments were undertaken towards developing the SCMoV genome into a VIGS vector. Three forms each of five major GFP chimeric constructs of pFL (the full length SCMoV cDNA clone) were generated from which in vitro- and in vivo-transcribed RNA transcripts could be derived. The rationale used in developing these constructs was gene insertion andlor replacement with d p , and duplication of the putative subgenomic RNA promoter (sgPro) of SCMoV. The major constructs were as follows: pFLCPgfp, pFL with the d p gene fused to the 3' end of the CP gene, pFLP 1 gfp, pFL with gj27 gene fused to the 3 ' end of the ORF 1, pFLCPsgprogfp, pFL with a putative sgPro sequence and a translatable & gene cloned in tandem between the CP gene and the 3' NCR of SCMoV, pFLCPVsgprogf$, pFL with a putative sgPro sequence and a translatable gfp gene cloned in tandem between a truncated CP gene and the 3' NCR and pFLREPsgprog@, pFL with the ORF2b, a putative sgPro sequence and a translatable &fP gene cloned in tandem between a truncated CP gene and the 3' NCR These constructs were all made, but a detailed assessment of their vector potential could not be done because there was a delay of about one year whilst the Office of the Gene Technology Regulator processed the application for permission for glasshouse testing. Although additional work needs to be undertaken to complete development of a final RNA silencing vector, this study has contributed to new knowledge in terms of extending understanding of SCMoV host range, symptoms, sequence variation and control of gene expression. The constructs made have also laid the groundwork for development of a legume gene silencing vector based on SCMoV.

Biserrula pelecinus L. has been introduced to Australia from the Mediterranean region, in the last decade due to many attractive agronomic features. This deep rooted, hard seeded, acid tolerant and insect resistant legume species provides high quality food for cattle and sheep, and grows well under the harsh edaphic and environmental conditions of Australia. In 1994, B. pelecinus was introduced to a site in Northam, Western Australia where there were no native rhizobia capable of nodulating this legume. The introduced plants were inoculated with a single inoculant strain of Mesorhizobium sp., WSM1271. This study investigated whether a diversity of rhizobia emerged over time. A second objective was to investigate the possible mechanisms involved in the diversification of rhizobia able to nodulate B. pelecinus. Eighty eight isolates of rhizobia were obtained from nodules on B. pelecinus growing at the Northam site in August 2000, six years after introduction. These plants were self-regenerating offspring from the original seeds sown. Molecular fingerprinting PCR with RPO1 and ERIC primers revealed that seven strains (novel isolates) had banding patterns distinct from WSM1271 while 81 strains had similar banding patterns to WSM1271. A 1400 bp internal fragment of the 16S rRNA gene was amplified and sequenced for four of the novel isolates (N17, N18, N45 and N87) and WSM1271. The phylogenetic tree developed using these sequences clustered the novel isolates in Mesorhizobium. There were >6 nucleotide mismatches between three of the novel isolates (N17, N18, N87) and WSM1271 while there were 23 nucleotide mismatches between N45 and WSM1271. When B. pelecinus cv. Casbah was inoculated with the novel isolates, five (N17, N18, N39, N46 and N87) yielded <40% of the shoot dry weight of the plants inoculated with the original inoculant (WSM1271). Novel isolates N15 and N45 were completely ineffective on B. pelecinus cv. Casbah. Physiological experiments to test the ability of the novel isolates and WSM1271 to grow on 14 different carbon sources (N acetyl glucosamine, arabinose, arbutine, dulcitol, β-gentiobiose, lactose, maltose, melibiose, D-raffinose, saccharose, L-sorbose, D-tagatose, trehalose and D-turanose) as the sole source of carbon, intrinsic resistance to eight different antibiotics (ampicillin, chloramphenicol, gentamicin, kanamycin, nalidixic acid, spectinomycin, streptomycin and tetracycline) and pH tolerance (pH 4.5, 5.0, 7.0, 9.0) revealed that the novel isolates had significantly different carbon source utilization patterns to WSM1271. However, pH tolerance and intrinsic resistance to antibiotics were similar between the novel isolates and WSM1271 except for streptomycin (100 μg/ml). Novel isolates N17, N18, N46 and N87 were susceptible for this antibiotic while the other novel isolates and WSM1271 were resistant. Host range experiments were performed for the novel isolates N17, N18, N45, N87, WSM1271 and two other root nodule bacteria (RNB) previously isolated from B. pelecinus growing in the Mediterranean region (WSM1284 and WSM1497) for twenty one legumes (Amorpha fruticosa, Astragalus adsurgens, Astragalus membranaceus, Astragalus sinicus, Biserrula pelecinus cv Casbah, Dorycnium hirsutum, Dorycnium rectum, Glycyrrhiza uralensis, Hedysarum spinosissimum, Leucaena leucocephala, Lotus corniculatus, Lotus edulis, Lotus glaber, Lotus maroccanus, Lotus ornithopodioides, Lotus parviflorus, Lotus pedunculatus, Lotus peregrinus, Lotus subbiflorus, Macroptilium atropurpureum, and Ornithopus sativus). Only isolate N17 have the same host range as WSM1271 in that they both nodulated B. pelecinus and A. membranaceus, while the other three novel isolates, WSM1284 and WSM1497 had a broader host range than WSM1271. Three isolates N18, N45 and N87 formed small white nodules on M. atropurpureum, in addition to nodulating the above hosts. Isolates N18 and N45 also nodulated A. adsurgens while N45 was the only isolate to nodulate L. edulis. Isolate N87 was the only isolate to nodulate A. fruticosa. WSM1497 nodulated A. adsurgens, A. membranaceus, B. pelecinus and L. corniculatus while WSM1284 was a promiscuous strain that nodulated 16 host species out of the 21 tested. A 710 bp internal region of nifH, a 567 bp internal region of nodA and a 1044 bp internal region of intS were sequenced for N17, N18, N45, N87 and WSM1271. The sequence comparison showed that the sequences of the above three genes of the four novel isolates were identical to that of WSM1271. Eckhardt gel electrophoresis revealed that WSM1271, three other RNB isolates from B. pelecinus from the Mediterranean region and isolate N18 each have a plasmid of approximately 500 kb while N17, N45 and N87 are plasmid free. Probing of the plasmid DNA from the Eckhardt gel with nifH and nodA probes indicated that these two genes were not located on the plasmid. Furthermore, the results of this study demonstrated that 92% of the nodules on B. pelecinus growing in the Northam site six years after the introduction of this plant were occupied by the inoculant strain and the N2 fixation efficiency of the progeny strains of WSM1271 remain similar to the mother culture. This study also showed that the carbon source utilization pattern, intrinsic antibiotic resistance and pH range of the progeny strains of WSM1271 remain relatively similar, except for few variations in carbon source utilization patterns. This thesis clearly demonstrated that phenotypicaly, genetically and phylogenetically diverse strains capable nodulating B. pelecinus evolved through symbiotic gene transfer from the inoculant strain to other soil bacteria within six years. The presence of intS, and the evidence of gene transfer between these Mesorhizobium strains indicates that transfer of symbiotic genes may have occurred via a symbiosis island present in WSM1271.