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Isolation and genetic dissection of an eukaryotic replicon that supports autonomous DNA replication

Maintenance of genome integrity requires that chromosomes be accurately and
faithfully replicated. We are using Tetrahymena thermophila as a model system for
studying the initiation and regulation of eukaryotic DNA replication. This organism
contains a diploid micronucleus and polyploid macronucleus. During macronuclear
development, the five diploid chromosomes of the micronucleus are fragmented into 280
macronuclear minichromosomes that are subsequently replicated to ~45 copies. In stark
contrast, the 21 kb ribosomal DNA minichromosome (rDNA) is amplified from 2 to
10,000 copies in the same nucleus. Previous characterization of the rDNA replicon has
led to the localization of its origin and the cis-acting regulatory determinants to the 1.9
kb 5'non-transcribed spacer region.
The objective of this study was to identify and characterize non-rDNA origins of
replication in Tetrahymena. This will help determine the underlying basis for differential
regulation of rDNA and non-rDNA origins during development, as well as provide a
better understanding of the organization of eukaryotic replicons. To this effect, I developed a DNA transformation assay that I used to isolate new Tetrahymena
replication origins. A 6.7 kb non-rDNA fragment, designated TtARS1, was shown to
support stable autonomous replication of circular plasmids in Tetrahymena. Genetic
dissection revealed that TtARS1 contains two independent replicons, TtARS1-A and
TtARS1-B. Full TtARS1-A function requires a minimal sequence of 700 bp, and two
small regions in this fragment have been shown to be essential for origin function.
TtARS1-B replicon function was localized to a 1.2 kb intergenic segment that contains
little sequence similarity to TtARS1-A. Both non-rDNA replicons lack sequence
similarity to the rDNA 5' NTS, suggesting that each replicon interact with a different set
of regulatory proteins. This study indicates that the rDNA and the non-rDNA replicons
have a modular organization, containing discrete, cis-acting replication determinants.

Identiferoai:union.ndltd.org:tamu.edu/oai:repository.tamu.edu:1969.1/4666
Date25 April 2007
CreatorsDatta, Shibani
ContributorsKapler, Geoffrey M.
PublisherTexas A&M University
Source SetsTexas A and M University
Languageen_US
Detected LanguageEnglish
TypeBook, Thesis, Electronic Thesis, text
Format1177316 bytes, electronic, application/pdf, born digital

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