For many cattle operations, profitability depends on the success of reproductive management programs. Opportunities for improving fertility exist within the numerous challenges related to reproductive management. Non-conventional, creative tools for reproductive management could help producers overcome these challenges. In an effort to produce information that could be used to improve reproductive performance of cattle, the following studies were undertaken. The objectives of these studies were threefold: to determine whether GnRH administered as an epidural injection causes ovulation in healthy cows and heifers, to evaluate whether the follicular environment (specifically, follicle fluid) surrounding the oocyte during the maturation phase affects the ability of the cumulus-oocyte complex to progress through early embryonic development, and to investigate the relative effects of estradiol and progesterone on oocyte maturation and early embryo development. Ability of GnRH to elicit an ovulatory response when administered as an epidural was evaluated in crossbred angus cows and heifers. The preliminary study evaluated this route of administration in crossbred angus cows. Animals were assigned randomly to either intramuscular or epidural administration, and ovaries were visualized via transrectal ultrasound every 6 h until ovulation of the dominant follicle. Results indicated that epidural administration of GnRH was able to trigger an ovulatory response, but timing of ovulation was not measured. The main experiment evaluated incidence of ovulation, time to ovulation, and ovulatory follicle size in crossbred angus heifers administered GnRH either epidurally or intramuscularly. Heifers were randomly assigned to treatment and ovaries were visualized every 4 h via transrectal ultrasound until ovulation of the dominant follicle. Results indicated that epidural administration of GnRH was able to elicit an ovulatory response in heifers, and the timing of ovulation and ovulatory follicle size was not different between administration route. Further investigation is needed to determine if characteristics of the ovulatory response (such as the luteinizing hormone surge) and circulating concentrations of GnRH are altered by epidural administration, which may impact fertility. GnRH administration is standard practice in many estrous synchronization programs. For fixed-time artificial insemination programs, the detection of estrus prior to insemination has been shown to improve conception and decrease early embryonic loss. The impact of behavioral estrus expression on the oocyte and early embryo were evaluated. Oocytes were matured in vitro in follicle fluid collected from synchronized cows who were classified as having expressed behavioral estrus or not expressing estrus. Embryo cleavage was not affected by estrus expression, but there was a tendency for improved blastocyst development in embryos matured in follicle fluid from animals who had expressed estrus. Cell number was not affected by estrus expression, but future research is needed as to the effect on oocyte acquisition of competence and early embryonic development. Despite the progress that has been made in culture conditions for in vitro produced embryos, developmental capacity following fertilization is limited at best, with only around one-third of oocytes placed into maturation resulting in viable embryos. During in vivo maturation, the oocyte undergoes final maturation within the follicle, surrounded by a changing microenvironment of estradiol and progesterone. Although the effects of steroids on oocyte development in vitro have been studied on an individual basis, a direct comparison between the ratio of estrogen and progesterone relative to follicle size has not been investigated Effects of steroid hormones estradiol and progesterone on oocyte maturation and early embryonic development were evaluated. Oocytes were matured in vitro in media supplemented with either estradiol, progesterone, or a combination of estradiol and progesterone. Oocytes were fertilized after maturation and cultured for 7 d until development to blastocyst stage. Addition of estradiol alone did not support oocyte maturation or early embryonic development in vitro, and a combination of estradiol and progesterone exhibited an inhibitory effect on oocyte maturation and early embryonic development. Addition of progesterone alone resulted in improved development when compared with estradiol alone or a combination of estradiol and progesterone. These results indicate that efficiency of reproductive management programs is controlled by multi-faceted factors and opportunities for improvement of reproductive outcomes exist in all of these factors. Although ovulation can be elicited via epidural administration, the impact of this ovulatory trigger on fertility requires further investigation. Display of estrus after synchronization for fixed-time artificial insemination improves conception and decreases early embryonic loss and has a may improve blastocyst development. This effect on early embryo development could be the focus of future research, further improving fertility and possibly the efficacy of in vitro embryo production. Steroid hormones play crucial roles in oocyte competency and the addition of progesterone during in vitro maturation improves development compared with estradiol alone or a combination of estradiol and progesterone. / Ph. D. / Reproductive success is critical for economic sustainability for many cattle operations. Creative tools for fertility management could help cattle producers overcome many challenges to fertility. In an effort to produce information that could be used to improve reproductive performance of cattle, the following studies were undertaken. The objective of these studies was to determine whether hormone administration as an epidural injection causes ovulation in healthy cattle (young and mature cattle assessed). Additionally, the second study evaluated whether the follicle (fluid-filled compartment surrounding the egg on the ovary) environment affects the female egg prior to ovulation, and the early embryo after fertilization. Finally, the third study looked at the impact of follicle fluid and specific hormones on embryo growth. An experiment was conducted in cows and heifers to determine if administering a hormone as an epidural injection, as opposed to conventional methods, could cause ovulation of the follicle. Animals received either an intramuscular or epidural hormone injection, and the ovaries of the animals were observed on an ultrasound until the follicle ruptured, releasing the egg. Epidural administration of the hormone was indeed able to trigger the rupture of the follicle. Hormone administration is standard practice in many cattle fertility programs. To maximize fertility, animals need to come into “heat” or estrus (period of sexual receptivity). Coming into heat is important for fertility in the female as it is indicative of impending ovulation and preparation of the egg for fertilization. In some reproductive management systems, reproductive cycles can be controlled in ways that deemphasize the need for behavioral estrus. Recent reports have suggested that animals in these systems that exhibit behavioral estrus are more fertile, as it makes it more likely for the female to conceive and stay pregnant compared to females who do not come into heat. The impact of heat on the female egg and early embryo of the cow has not been investigated. To evaluate the impact of heat on embryos, eggs were taken from the ovary of the cow and matured in a cell culture lab overnight in media containing fluid taken from the follicles of animals who came into heat, and animals that did not come into heat. The eggs were then fertilized, and embryos developed. There was only a tendency for improvement in embryo development for those matured in fluid from animals in heat compared with animals not in heat. When growing embryos in a culture lab, success rates are lower than embryos developing in the animal. When the egg is being prepared for release, it goes through important maturation steps to enable fertilization and eventual growth into a calf. Hormones in the follicle fluid facilitate maturation, and the conditions in the follicle are not easily replicated in the lab. The addition of these critical hormones to the lab conditions may help facilitate improved development in lab-produced embryos. Two hormones (estrogen and progesterone) were added to follicle fluid that was used in the lab culture environment to determine their effect on embryo growth. When progesterone was added, embryos grew well, matching the development rate of the control medium. When estrogen was added, embryos experienced poor development. Neither resulted in embryo development that exceeded the control medium. These results indicate that control of reproduction in cattle is complex, and multiple opportunities exist to improve fertility. Future research on how the oocyte and embryo react to their environment is needed and will facilitate further improvement of reproductive management systems in cattle. Improved reproductive management will enhance efficiency, sustainability and profitability of cattle production systems.

The pharmacological development of non-steroidal contraceptives has yet to be achieved. Arresting oocyte maturation without blocking ovulation has been evaluated using different inhibitors of the phosphodiesterase 3A (PDE3A). Unfortunately, PDE3A is also expressed in the heart and blood vessels, and inhibition of PDE3A in oocytes can produce cardiovascular side effects. We reviewed the literature on available PDE3 inhibitors and selected cilostazol (CLZ), which is an FDA approved therapeutic. CLZ has the ability to decrease cellular adenosine uptake and consequently antagonizes side effects of PDE3A inhibition in vital organs. CLZ inhibited oocyte meiotic maturation in vitro. CLZ has more degenerative impact on arrested oocytes than matured oocytes, indicating that prolonged meiotic arrest of oocytes is harmful. Administration of CLZ any time from 9h before the ovulatory stimulus to 4h after the stimulus resulted in ovulation of immature oocytes. Controlling CLZ dose, time of CLZ administration, and time of oocyte collection resulted in ovulation of oocytes at different meiotic stages. Oral administrations of CLZ in naturally cycling mice were also observed to block pregnancy whereas remating of those previously treated females resulted in normal offspring and litter sizes. Therefore, CLZ does not only have a wide margin of contraception but also is reversible. Ovulated immature oocytes were observed to have higher rates of advanced chromatin configuration and cortical granule distribution, normal spindle and chromosomal organization, maturation, and in vitro fertilization (IVF) than ovarian immature oocytes. Ovulated metaphase I oocytes that were matured in vitro or in vivo had higher IVF rates than ovulated mature oocytes. Ovulated germinal vesicle (GV) oocytes that were in vitro matured also showed higher IVF rates but when in vivo matured, they had lower IVF rates than ovulated mature oocytes because of the high degeneration and low fertilization rates associated with in vivo maturation of GV oocytes. In summary, CLZ merits further evaluation as a non-steroidal contraceptive and is capable of producing oocytes of various meiotic stages with advanced developmental features.

During female meiotic prophase in many organisms, a specialized chromatin structure is formed in the oocyte nucleus. This structure is known as the karyosome, and has been proposed to be important for the formation of the female meiotic bipolar spindle. However, how the karyosome is formed and maintained is not very well understood. To identify proteins involved in the formation and maintenance of the karyosome, I carried out a cytological screen on a collection of 220 mutant fly lines for mutants that were defective in karyosome morphology. The screen identified 46 mutants on the X and 2nd chromosome with abnormal karyosomes. Genetic analysis of these 46 mutants, followed by molecular analysis of one mutant, identified SRPK (SR Protein Kinase) as a protein that is important for the proper formation of the karyosome. NHK-1 (Nucleosomal Histone Kinase 1) was previously identified as a protein that is essential for the formation of the karyosome via its phosphorylation of BAF (Barrier-to-Autointegration Factor). NHK-1 phosphorylation of BAF leads to the release of chromatin from the nuclear membrane, an essential step for the formation of the karyosome, however, the regulation of this process is unclear. In order to identify genes that interact with NHK-1, I carried out a genetic modifier screen using a semi-lethal allele of NHK-1, NHK-1trip. After screening a collection of 44 deficiencies located on the 2nd chromosome, I identified a genetic region (44B8-44D1) containing a gene that interacts with NHK-1 and, when gene dosage is halved, enhanced the semi-lethal phenotype of NHK-1trip.

Thesis advisor: Laura E. Hake / Metazoan development depends on cytoplasmic polyadenylation, a key mechanism that controls the translation of maternally deposited mRNAs. In Xenopus laevis oocytes, CPEB regulates the translation of several developmentally important mRNAs, which drive meiotic progression and the production of fertilizable eggs. Most of our current knowledge of this process, also referred to as oocyte maturation, has been acquired from experiments conducted in Xenopus laevis oocytes. Despite over 30 years of research devoted to the exploration of progesterone signaling during maturation, the very early events that occur from progesterone receptor engagement to CPEB activation are not well understood. XGef, a putative Rho family guanine nucleotide exchange factor (GEF), interacts with CPEB and facilitates CPEB activation and timely meiotic progression. To further our understanding of XGef function during meiotic progression, the requirement for exchange factor activity and the activities of several Rho GTPases during maturation were examined. Despite previous reports of XGef activation of Cdc42 in mammalian cell culture, XGef does not stimulate the activation of Cdc42 in maturing Xenopus oocytes. Further, Cdc42 activity does not affect CPEB phosphorylation and overexpression of a dominant negative Cdc42 mutant does not affect maturation. Inhibition of Toxin B sensitive Rho GTPases, including Cdc42, Rac1 and Rho A-C, also fails to affect CPEB activation or meiotic progression. Lastly, the overexpression of XGef exchange deficient point mutants did not affect maturation compared to oocytes overexpressing wildtype XGef. Together, these results suggest that as a facilitator of CPEB activation and meiotic progression, XGef functions independently of exchange factor activity and Rho GTPase activation. Additionally, we found that XGef activity influences the function of RINGO/CDK1, a novel component of the progesterone signaling pathway. XGef inhibition depresses RINGO-induced GVBD, whereas XGef overexpression enhances this process. XGef interacts with RINGO in oocyte extracts and the interaction is direct in vitro. Our protein interaction data, in total, suggest that a XGef/RINGO/MAPK/CPEB complex forms in ovo to facilitate CPEB activation. Lastly, inhibition of RINGO activity directly compromises CPEB phosphorylation during early maturation, which suggests that RINGO/CDK1 directly mediates CPEB-activation. / Thesis (PhD) — Boston College, 2009. / Submitted to: Boston College. Graduate School of Arts and Sciences. / Discipline: Biology.

The primordial follicle pool is the main source of developing follicles in the ovary. The length of reproductive life and the onset of menopause are governed by the amount of primordial follicles in the ovary. The genetic factors and molecular mechanisms that maintain the primordial follicles in a dormant and surviving state for the whole of reproductive life are not well understood. The phosphatidylinositol 3 kinase (PI3K) signaling pathways in the oocyte that control oocyte growth and early follicular development are largely unknown. The major aim of this thesis was to investigate the functional role of the intra-oocyte PI3K pathway in the regulation of primordial follicle activation and survival.  Phosphatase and tensin homolog deleted on chromosome ten (PTEN) is a major negative regulator of PI3K. The conditional deletion of Pten in the oocytes of primordial follicles led to the overgrowth of oocytes and activation of the entire pool of primordial follicles. There were higher numbers of activated primordial follicles at postnatal day 8 (PD8) in ovaries lacking PTEN in oocytes; by PD35 all the primordial follicles were activated and all the follicles were depleted by 12 weeks, causing premature ovarian failure (POF). In addition, the rate of follicular death that occurs during sexual maturity is reduced in ovaries that lack PTEN in oocytes. Further mechanistic studies revealed that loss of Pten in oocytes resulted in elevated Akt signaling and upregulation of both expression and activation of ribosomal protein S6 (rpS6). The overactivation of primordial follicles in ovaries that lack PTEN in oocytes is believed to be due to elevated expression and activation of rpS6. PTEN in oocytes is indispensable for the maintenance of primordial follicles in dormancy.  To study the role of the intra-oocyte PI3K signaling pathway in controlling the survival and maintenance of primordial follicles, 3-phosphoinositide-dependent protein kinase-1 (PDK1) was deleted in oocytes of primordial follicle. The loss of Pdk1 in oocytes led to the depletion of most primordial follicles around the onset of sexual maturity, causing POF during early adulthood. Furthermore, the activation of Akt, p70 S6 kinase 1 (S6K1), and rpS6 was impaired in oocytes that lacked PDK1. The suppressed PDK1–Akt–S6K1–rpS6 signaling in oocytes appears to be responsible for the loss of primordial follicles. The excessive activation of primordial follicles seen in the absence of Pten in oocytes could be reversed by concurrent deletion of Pdk1. In addition, the elevated activation of Akt and S6K1 in the absence of PTEN in oocytes was not observed in PTEN and PDK1 double mutant mice. Similarly, the hyperphosphorylation of rpS6 in oocytes that lack PTEN was prevented in double mutant mice, which was most likely due to downregulation of S6K1 activation. Thus, inactivation of rpS6 in double mutant mice might be the reason for the prevention of excessive primordial follicular activation and survival.  PTEN and PDK1 in oocytes are essential for the maintenance of quiescence and survival of primordial follicles. The molecular network involving PI3K/PTEN–PDK1 signaling in oocyte controls the survival, loss, and activation of primordial follicles, which together govern reproductive aging and determine the length of reproductive life in females. The results of the above studies indicate that the mammalian oocyte serves as the seat of programming of follicular activation and survival.

Decline in fertility with age has been well documented in women. There are ethical limitations to use humans as a model for basic research, and there is a lack of well characterized animal model. The objective was to characterize and validate a bovine model for the study of age-associated subfertility. All experiments were conducted on the same group of 13-14 year old cows (n=10), and their 1-4 year old young daughters (n=10). Mother-daughter pairs were used to reduce genetic variations. <p>Follicular wave pattern in a natural reproductive cycle was maintained in old cows similar to that in daughters. We hypothesized that aging in cattle is associated with elevated circulating concentrations of FSH, and reduced concentrations of steroid hormones. As stated, circulating FSH concentrations were higher (P=0.009) during follicular waves in old than young cows. The ovulatory follicle in 2-wave cycles was smaller in old cows (P=0.04), but plasma estradiol concentrations were higher (P=0.01). Luteal phase progesterone tended to be lower in old than young cows (P=0.1). The number of 4-5 mm follicles recruited into a follicular wave was lower (P<0.05) in old cows than in their daughters.<p>The response to ovarian synchronization and superstimulatory treatments was compared between old and young cows. We hypothesized that aging in cattle is associated with decreased synchrony of an induced follicular wave after steroid treatment. Conversely, the emergence of an induced follicular wave was synchronous between age groups. The preovulatory LH surge was delayed in old compared to young cows (P=0.01), but the detected ovulation times were not different. Old cows had fewer (P<0.01) follicles equal or greater than 6 mm after superstimulation, and tended (P=0.1) to have fewer ovulations than their daughters (32±4 versus 40 ±3, respectively). The response of individual cows to successive superstimulatory treatments was correlated (r>0.8; P<0.0001). <p>The hypothesis of reduced oocyte developmental competence in old cows was tested by comparing embryo production and pregnancy rates between old and young cows. Fewer (P=0.04) embryos were recovered from old cows (6±2) than their daughters (12±2). A higher proportion (P<0.01) of unfertilized oocytes and/or uncleaved zygotes were recovered from old cows (222/312, 71%) than their daughters (119/316, 38%). The recovery of fewer embryos in old cows suggests reduced oocyte developmental competence. The survival of embryos after transfer into unrelated young recipients was similar between age groups. <p>The effects of advanced age on oocyte meiotic maturation and oocyte chromosome numbers abnormalities were studied in old and young cows. Our hypothesis of compromised oocyte meiotic maturation with age was not supported; similar or higher proportion of metaphase II oocytes were recovered from old than young cows. The abnormalities of oocyte chromosomal numbers were similar between age groups. <p>To conclude, endocrine, follicular and oocyte developmental changes in old cows are consistent with those reported for women approaching menopause. Therefore, our results validated the use of a bovine model to study age-associated subfertility in women. Unlike women, we did not detect an age-related increase in abnormalities of oocyte chromosome numbers in cattle.

Decline in fertility with age has been well documented in women. There are ethical limitations to use humans as a model for basic research, and there is a lack of well characterized animal model. The objective was to characterize and validate a bovine model for the study of age-associated subfertility. All experiments were conducted on the same group of 13-14 year old cows (n=10), and their 1-4 year old young daughters (n=10). Mother-daughter pairs were used to reduce genetic variations. <p>Follicular wave pattern in a natural reproductive cycle was maintained in old cows similar to that in daughters. We hypothesized that aging in cattle is associated with elevated circulating concentrations of FSH, and reduced concentrations of steroid hormones. As stated, circulating FSH concentrations were higher (P=0.009) during follicular waves in old than young cows. The ovulatory follicle in 2-wave cycles was smaller in old cows (P=0.04), but plasma estradiol concentrations were higher (P=0.01). Luteal phase progesterone tended to be lower in old than young cows (P=0.1). The number of 4-5 mm follicles recruited into a follicular wave was lower (P<0.05) in old cows than in their daughters.<p>The response to ovarian synchronization and superstimulatory treatments was compared between old and young cows. We hypothesized that aging in cattle is associated with decreased synchrony of an induced follicular wave after steroid treatment. Conversely, the emergence of an induced follicular wave was synchronous between age groups. The preovulatory LH surge was delayed in old compared to young cows (P=0.01), but the detected ovulation times were not different. Old cows had fewer (P<0.01) follicles equal or greater than 6 mm after superstimulation, and tended (P=0.1) to have fewer ovulations than their daughters (32±4 versus 40 ±3, respectively). The response of individual cows to successive superstimulatory treatments was correlated (r>0.8; P<0.0001). <p>The hypothesis of reduced oocyte developmental competence in old cows was tested by comparing embryo production and pregnancy rates between old and young cows. Fewer (P=0.04) embryos were recovered from old cows (6±2) than their daughters (12±2). A higher proportion (P<0.01) of unfertilized oocytes and/or uncleaved zygotes were recovered from old cows (222/312, 71%) than their daughters (119/316, 38%). The recovery of fewer embryos in old cows suggests reduced oocyte developmental competence. The survival of embryos after transfer into unrelated young recipients was similar between age groups. <p>The effects of advanced age on oocyte meiotic maturation and oocyte chromosome numbers abnormalities were studied in old and young cows. Our hypothesis of compromised oocyte meiotic maturation with age was not supported; similar or higher proportion of metaphase II oocytes were recovered from old than young cows. The abnormalities of oocyte chromosomal numbers were similar between age groups. <p>To conclude, endocrine, follicular and oocyte developmental changes in old cows are consistent with those reported for women approaching menopause. Therefore, our results validated the use of a bovine model to study age-associated subfertility in women. Unlike women, we did not detect an age-related increase in abnormalities of oocyte chromosome numbers in cattle.

Horse owners commonly maintain their broodmares in training and competition during the breeding season. The effect this has on mare reproductive efficiency has received limited attention. Heat stress has shown to be detrimental to oocyte competence in other species and heat shock protein 70 has been shown to be an important gene in regulating cellular response to heat. Mares were exercised in a hot humid environment to determine the effects on reproductive efficiency. Embryos were collected at d 7 after ovulation from exercised and control mares. Oocyte developmental competence was measured after oocytes were subjected to a one time heat shock, 42 ºC for 2 or 4 h, at the onset or near completion of in vitro maturation. Embryos from both previous experiments were examined for HSP70 gene expression by real time RT-PCR. Exercised mares ovulated significantly smaller follicles, 39.8 vs. 41.5 mm diameter, and ovulated later after being given PGF2α, 8.5 vs. 9.2 d. Twenty-two embryos (22/35) were recovered from control mares, recovery rate of 63%. Significantly fewer embryos were recovered in exercised mares (11/32), recovery rate of 34%. A lower proportion of grade 1 embryos were recovered from exercised versus control mares (4/11 vs.16/22,respectively). No effect was observed on oocyte nuclear maturation or embryonic development after ICSI when oocytes were exposed to heat shock at the onset of IVM. A heat shock of 42 ºC for 2 or 4 h on oocytes during late IVM resulted, however, in a significantly lower rate of nuclear maturation, and a significant decrease in advanced embryo development (morulae plus blastocysts). Heat shock protein 70 gene expression was shown to be related to quality score of in vivo-recovered embryos, with lower quality embryos recording a significantly higher relative expression. Heat shock of late stage IVM oocytes for 4 h resulted in significantly higher blastocyst HSP70 expression. Results of this study indicate that exercise in a hot humid environment is detrimental to mare reproductive efficiency, late-stage maturing oocytes are sensitive to heat, and HSP70 expression in equine embryos is related to embryo quality score and oocyte quality.

Prenatal mortality in the swine ranges from 30%~40%. Little is known about genes that involve in the preovulation events that the initiation of swine oocyte development. The main objective of this study was to utilize suppression subtractive hybridization¡]SSH¡^to delineate the differential gene expression between in vitro culture mature and antral-follicle oocytes of swine development. The knowledge of genes and their accumulated mRNA is essential to better understand the mechanisms involved in the oocyte maturation and the survival of the in vitro produced embryos. Porcine ovaries obtained from the slaughterhouse were used to collect oocytes from follicle with a diameter ≥ 3 mm. After in vitro mature for two days, oocytes with first polar body were subjected to as the testers and were lysed for mRNA extraction. Pools of 26 denuded oocytes without culture were submitted to suppressive subtraction hybridization (SSH) as the drivers. Forward and reverse subtractions were performed to identify candidate genes differentially expressed between in vitro culture mature and primordial-follicle oocytes. A total of one hundred and thirty-five differential expressed plasmid clones were sequenced, and each was analyzed by BLAST programs. Of these transcripts, 40 clones were subjected to differential screening by a dot blot cDNA array. We identified three genes like zona pellucida glycoprotein (ZP1), 1-aminocyclopropane-1-carboxylate synthase (ACS), and death associated protein 5¡]DAP 5¡^while other numerous clones remain novel. The in vivo functions of the genes remain further investigation.

The progress of studies on genes concerning the development and differentiation of early swine embryos have been delayed by limited paucity material. In order to identify the porcine ESTs associates with promoting its breeding efficiency, a cDNA library and ESTs database from oocytes of high reproductive swine is established. Oocytes were obtained from Duroc pig by superovulation which was performed by Taiwan Livestock Research Institute, Council of Agriculture. Total RNA was isolated from 50 mature oocytes, reverse transcription is then performed, followed by PCR based amplification of the cDNA. The amplified cDNA size ranges from 0.4 to 5 kb. The derived cDNA were ligated to a pCR2.1 vector, and the library has complexities of about 5.26¡Ñ104 independent clones. A total of 320 clones was picked and sequenced. By BLASTx analysis, among the 123 sequences, more than 43.07%¡]53/123¡^ mitochondrial proteins are found, 56.91¢H¡]70/123¡^ of the sequence were homologous to known transcripts from human, mouse, Drosophila. In nucleotide level analysis, 82.11¢H¡]101/123¡^ matched with the mitochondrial, ribosome genes and 17.89¢H¡]22/123¡^matched with other homologous genes by BLASTn. PCR analysis of the oocyte library for specific genes revealed transcripts for genes including homologous genes¡]2 pairs highly abundance and 2 pairs low abundance genes¡^, housekeeping genes¡]ACT£] and G3PDH¡^ and developmental genes¡]NEK2 and ZP1¡^. However, novel genes of swine are supposed to be the candidates for high productive phenotypes of swine. The library is a valuable resource for the isolation of clones representing genes active at the early stage. The ability to construct cDNA expression library from a few cells will allow gene expression analysis from oocyte biopsies and derived by nuclear transfer procedures.