Gamete Production Research Articles

Genomic affinity in hybrids of B-genome Arachis species: new genetic resources toward peanut improvement

Abstract Peanut (Arachis hypogaea L.) is an important oilseed crop and food legume that is highly susceptible to biotic and abiotic factors. Wild Arachis species represent useful genetic resources because of their resistance to pests and diseases. In particular, understanding the affinity between B-genome species is important for broadening the genetic base of A. hypogaea (AABB genome), since only one population of A. ipaensis is known, and relatively few other species have been described. Therefore, we aimed to determine the genomic affinity between A. ipaensis and A. williamsii by developing hybrids. Microsatellite markers verified the hybrid status, and chromosome pairing and pollen viability results revealed that the species share high genomic affinity. Additionally, the presence of dyads detected in sporad and pollen analyses indicated the production of 2n gametes. These results will be useful for performing evolutionary studies and developing strategies for introgression programs to improve the B genome of A. hypogaea.

The Endocrine Function of Testes in 12- and 18-Month-Old Boars of Different Breeds.

Testes have several primary functions, such as male gametes production (spermatozoa) and secretion of several endocrine factors, including the production of steroid and protein hormones which facilitate elements in the healthy reproductive function of mammals. The potential of an animal functional endocrine reservoir could be an interesting finding in animal reproduction management. Therefore, the current study aimed to analyze the functional endocrine reserves of testes in 12- and 18-month-old boars of four different boar breeds, namely Large White, Landrace, Duroc, and Tempo, as the animal model in this research (n=10). To determine the functional endocrine reserves of the testes at 12 and 18 months of age, boars received injections of human chorionic gonadotropin (hCG) 3 times every 72 hours. Testosterone was measured in blood samples (10 mL) taken from the jugular vein before the administration of hCG as well as 2, 12, 24, 48, and 72 hours after administration of each of three hCG injections. The index of endocrine activity of the testes was determined by the formula: Ita = T1 -T0 / T0 , where Ita is the index of endocrine activity of the testes, T0 is the testosterone concentration before the administration of hCG, and T1 is the maximum testosterone concentration after the third administration of hCG. The effects of the hCG injection on boar testes at different age periods indicated that the testes of Large White and Duroc boars have higher potential endocrine reserves compared with the Landrace and Tempo breeds.

Detection of Ovarian Tumor Using Machine Learning Approaches A Review

The important part of female reproductive system is ovaries. The importance of these tiny glands is derived from the production of female sex hormones and female gametes. The place of these ductless almond shaped tiny glandular organs is on just opposite sides of uterus attached with ovarian ligament. There are several reasons due to which ovarian cancer can arise but it can be classified by using different number of techniques. Early prediction of ovarian cancer will decrease its progress rate and may possibly save countless lives. CAD systems (Computer-aided diagnosis) is a noninvasive routine for finding ovarian cancer in its initial stages of cancer which can keep away patients’ anxiety and unnecessary biopsy. This review paper states us about how we can use different techniques to classify the ovarian cancer tumor. In this survey effort we have also deliberate about the comparison of different machine learning algorithms like K-Nearest Neighbor, Support Vector Machine and deep learning techniques used in classification process of ovarian cancer. Later comparing the different techniques for this type of cancer detection, it gives the impression that Deep Learning Technique has provided good results and come out with good accuracy and other performance metrics.

Transferrin receptor (TFRC) is essential for meiotic progression during mouse spermatogenesis.

Meiosis is a highly conserved process, and is responsible for the production of haploid gametes and generation of genetic diversity. We previously identified the transferrin receptor (TFRC) in the proteome profile of mice neonatal testes, indicating the involvement of the TFRC in meiosis. However, the exact molecular role of the TFRC in meiosis remains unclear. In this study, we aimed to determine the function of the TFRC in neonatal testicular development by TFRC knockdown using the testis culture platform. Our results showed high TFRC expression in 2-week testes, corresponding to the first meiotic division. Targeting TFRC using morpholino oligonucleotides resulted in clear spermatocyte apoptosis. In addition, we used the chromosomal spread technique to show that a deficiency of TFRC caused the accumulation of leptotene and zygotene spermatocytes, and a decrease of pachytene spermatocytes, indicating early meiotic arrest. Moreover, the chromosomes of TFRC-deficient pachytene spermatocytes displayed sustained γH2AX association, as well as SYCP1/SYCP3 dissociation beyond the sex body. Therefore, our results demonstrated that the TFRC is essential for the progression of spermatocyte meiosis, particularly for DNA double-stranded break repair and chromosomal synapsis.

DNA Damaged Induced Cell Death in Oocytes.

The production of haploid gametes through meiosis is central to the principle of sexual reproduction. The genetic diversity is further enhanced by exchange of genetic material between homologous chromosomes by the crossover mechanism. This mechanism not only requires correct pairing of homologous chromosomes but also efficient repair of the induced DNA double-strand breaks. Oocytes have evolved a unique quality control system that eliminates cells if chromosomes do not correctly align or if DNA repair is not possible. Central to this monitoring system that is conserved from nematodes and fruit fly to humans is the p53 protein family, and in vertebrates in particular p63. In mammals, oocytes are stored for a long time in the prophase of meiosis I which, in humans, can last more than 50 years. During the entire time of this arrest phase, the DNA damage checkpoint remains active. The treatment of female cancer patients with DNA damaging irradiation or chemotherapeutics activates this checkpoint and results in elimination of the oocyte pool causing premature menopause and infertility. Here, we review the molecular mechanisms of this quality control system and discuss potential therapeutic intervention for the preservation of the oocyte pool during chemotherapy.

Effects of anesthetic MS-222 on stress and reproduction of South American silver catfish (Rhamdia quelen) males

Anesthesia is a common practice used in fish research and aquaculture. It is important to understand anesthetic effects on the animal and tissues of interest to ensure validity of data and to improve animal welfare in research and fish production endeavors. The production of some captive fish species is only possible by imposing artificial reproduction procedures, and manipulation of fish for these purposes is a stressor. The purpose of this study, therefore, was to evaluate effects of different concentrations (100, 200, and 300 mg/L) of the anesthetic MS-222 (tricaine methanesulfonate) on cortisol concentrations and effects on sperm quality in Rhamdia quelen. After hormonal induction of gamete production, 28 sexually mature males were randomly assigned to treatments, and milt and blood samples were collected. Anesthesia induction time, motility rate, sperm concentration and morphology, plasma cortisol concentrations, and reproductive hormone concentrations (testosterone, 17-α-hydroxyprogesterone, and estradiol) were evaluated. Sperm motility was greater in the control than 300 mg/L treatment group but did not differ among the control, 100, and 200 mg/L groups. The estradiol concentration was greater in non- anesthetized than anesthetized Rhamdia quelen, but plasma cortisol concentrations did not differ among treatment groups (182.50 ± 42.03 ng/mL). The anesthetic MS-222 at concentrations of 100, 200, and 300 mg/L did not inhibit the stress response due to handling of Rhamdia quelen males. In addition, treatment with MS-222 was not effective in inhibiting detrimental effects on sperm quality because this treatment was associated with impaired sperm motility and lesser concentrations of plasma estradiol.

Angelika Amon.

Angelika Amon.

Reproductive and genetic roles of the maternal progenitor in the origin of common wheat (Triticum aestivum L.).

Common wheat (Triticum aestivum L., AABBDD genome) is thought to have emerged through natural hybridization between Triticum turgidum L. (AABB genome) and Aegilops tauschii Coss. (DD genome). Hybridization barriers and doubling of the trihaploid F1 hybrids’ genome (ABD) via unreduced gamete fusion had key roles in the process. However, how T. turgidum, the maternal progenitor, was involved in these mechanisms remains unknown. An artificial cross‐experiment using 46 cultivated and 31 wild T. turgidum accessions and a single Ae. tauschii tester with a very short genetic distance to the common wheat D genome was conducted. Cytological and quantitative trait locus analyses of F1 hybrid genome doubling were performed. The crossability and ability to cause hybrid inviability did not greatly differ between the cultivars and wild accessions. The ability to cause hybrid genome doubling was higher in the cultivars. Three novel T. turgidum loci for hybrid genome doubling, which influenced unreduced gamete production in F1 hybrids, were identified. Cultivated T. turgidum might have increased the probability of the emergence of common wheat through its enhanced ability to cause genome doubling in F1 hybrids with Ae. tauschii. The ability enhancement might have involved alterations at a relatively small number of loci.

Effect of oral administration of a mixture of pyrethroids at doses relevant to human exposure on the general and male reproductive physiology in the rat

Studies on the effects of unintentional intake of pyrethroid pesticides that are akin to actual human exposure settings are very rare. Such an exposure is primarily by consuming the food products as routine diet that contain residual levels of pyrethroids. In this study, rats were orally administered for 15 months with a mixture of pyrethroids at a dose that is one-fifth (high dose; HD) or one-twenty fifth (low dose; LD) of the residual levels commonly present in the average amount of rice and vegetables consumed by Indian population. Lipid profile, kidney and liver function were assessed. Lipid peroxidation, nitric oxide, antioxidant enzyme activities and histopathological changes were analyzed in the liver, lung, kidney, pancreas, testes, caput, cauda and prostate. The effect on the male reproductive system as a function of sperm count, enzyme activity of 3β-HSD and 17β-HSD and the expression profile of genes involved in spermatogenesis, steroidogenesis, genetic reprogramming and apoptosis of male gametes were evaluated. Significant increase in the relative organ weight, perturbations in the activities of antioxidant enzymes, lipid profile and liver function were observed in both LD and HD groups. Damage to the anatomical architecture was evident in all the tissues due to pyrethroid toxicity. Exposure to LD and HD of pyrethroid mixture resulted in decreased sperm count, activities of 3β-HSD and 17β-HSD, impaired capacitation and acrosome reaction and perturbations in the expression of genes that govern male gamete production. Results of our study indicate that exposure to pyrethroids for longer durations even at doses that are far below the residual levels present in the food consumed will result in severe damage to general physiological processes as well as reproductive function.

PSII-23 Aflatoxin B1 influences expression of TRPM8 in SKOV, ovarian epithelial cancer cells

Abstract Aflatoxins are mold products of Aspergillus flavus. They are common food contaminants that affect dietary staples. Aflatoxins are most prevalent in emerging countries and negatively impact the health and reproduction of several animals. Aflatoxin B1 (AFB1) affects fertility in many species by decreasing the number of gametes. The mechanism for aflatoxin’s effect on gamete production has not been fully elucidated. In aflatoxin treated rats, steroidogenesis is affected by the competitive binding of aflatoxin to the StAR protein. The transient receptor potential melastatin 8 (TRPM8) is a nonselective cation channel highly expressed in male reproductive tracts, and sheep ovaries. TRPM8 binds testosterone and is responsive to steroids. The objective of these experiments is to determine if AFB1 influenced the expression of TRPM8 channels in an ovarian cell line. Human epithelial ovarian cells, SKOV, were seeded into chamber slides and treated in triplicate with media containing ethanol, 5µg/ml AFB1, 10µg/ml AFB1, or 20µg/ml AFB1 for 24 hours. The cells were stained for TRPM8 using immunocytochemistry and in a replicate experiment, analyzed for mRNA using Real Time RT-PCR protocols. Images were captured at 200x magnification and analyzed. Mean gray scale intensity was used to determine staining intensity as a reflection of TRPM8 expression. SKOV cells treated with AFB1 had increased staining (P ≤ 0.001) compared to ethanol treated cells. Relative TRPM8 mRNA did not differ with AFB1 treatments (P = 0.2). Inconsistency between mRNA and protein expression may be due to the timing of mRNA synthesis and translation of the protein. Based on these results, expression of TRPM8 in SKOV cells increased in response to AFB1. Although it is not certain if this effect is restricted to these transformed cells, the possibility remains that changes in TRPM8 expression may contribute to the negative reproductive consequences of AFB1 exposure in humans and livestock species.

Gonadal steroid fluctuations and reproduction results of European grayling (Thymallus thymallus L.) from broodstock farmed in a recirculation aquaculture system

The initial experiment of this study was conducted to determine whether sex steroid concentrations varied before, during and after the reproductive season of European grayling (Thymallus thymallus L.) farmed broodstock confined in a recirculation aquaculture system (RAS). The results indicated that the plasma sex steroid (testosterone - T, progesterone - P4 and estradiol - E2) concentrations varied (P < 0.05) during these reproductive periods. There were greater concentrations of T, P4 and E2 before and during the grayling reproductive season indicating there are important functions of these steroid hormones associated with gonadal maturation, gamete production and reproductive behavior during the spawning period. In the second experiment of this study, the effectiveness of European grayling controlled reproduction treatment regimens was analyzed and there were 34.69 % and 68.18 % having ovulations in the 2 and 3-year-old broodfish, respectively. Of the embryos developing to the eyed-egg stage, there were 3.70 % and 6.87 % derived from eggs of 2- and 3-year-old grayling females, respectively. Proportions of embryos developing from the eyed-egg stage to hatching were 38.1 % and 52.1 % from eggs of 2- and 3-year-old grayling females, respectively, when there was culturing in a RAS. The results indicate that with grayling broodfish there is greater efficacy in induction of reproduction when there is imposing of the controlled reproduction treatment regimen on 3- rather than 2-year-old broodfish.

Short-term testosterone use in female mice does not impair fertilizability of eggs: implications for the fertility care of transgender males.

Does testosterone use in females affect reproductive potential, particularly with regard to the production of fertilizable gametes? Testosterone (T) injections given to post-pubertal female mice caused virilization and although the ovaries were smaller than controls they were still responsive and produced fertilizable eggs when superovulated. Studies to examine the effects of testosterone on reproductive potential in transgender males are lacking. Recently, a model was developed that simulates many aspects of testosterone use in transgender males in order to look at reproductive effects of testosterone in female mice. This study found masculinizing effects on the mice but did not find significant deficits on the number of ovarian follicles; however, effects of testosterone use on ovarian stimulation and fertilizability of oocytes were not investigated. A total of 66, 6-week-old Hsd:NSA (CF-1) female mice and six Hsd:ICR (CD-1) male mice were used for this study. Mice were injected s.c. with 400 µg T or sesame oil once a week for 6 weeks and were either killed 1 week after the sixth injection (active exposure group), or 6-7 weeks after the final T injection (washout group). Both active exposure and washout groups were further subdivided into three groups: unstimulated, equine CG (eCG)-stimulated or eCG/hCG-stimulated. eCG-stimulated mice were killed 44-48 h after eCG injection. eCG/hCG-stimulated mice were injected with eCG, followed 48 h later with hCG. Mice were killed ∼13-18 h after the hCG injection. Data collected included daily vaginal cytology, terminal testosterone levels, ovary weights and histology, number of oocytes/eggs collected in each group, and cleavage to the two-cell stage following IVF. Testosterone-treated mice had testosterone levels elevated to the level of male mice and ceased cycling. Ovaries were significantly smaller in testosterone-treated mice, but they contained normal cohorts of follicles and responded to gonadotrophin stimulation by ovulating similar numbers of eggs as controls, that fertilized and cleaved in vitro. Mice were treated for only 6 weeks, whereas many transgender men use testosterone for many years before considering biological children, and developmental competence was not assessed. Importantly, a mouse system may not perfectly simulate human reproductive physiology. The current standard of care for transgender men who desire biological children is to cease testosterone therapy prior to ovarian stimulation, but the necessity for stopping testosterone is not known. Our model demonstrates that it is possible for testosterone-suppressed ovaries to respond to gonadotrophic stimulation by producing and ovulating fertilizable eggs, thereby obviating the need for testosterone cessation prior to ovarian stimulation. In time, these results may provide insights for future clinical trials of fertility treatment options for transgender men. This study was funded by the Reproductive Endocrinology and Infertility fellowship program through UConn Health Graduate Medical Education (to C.B.B.). The authors have no competing interests. N/A.

Differences in spawning time drive cryptic speciation in the coral Acropora divaricata

Most of the reef-building Acropora corals around Okinawa Island spawn in May and/or June. We found that two morphotypes of Acropora divaricata spawned in August and/or September. The “robust” and “slender” morphotypes differed in branch width and in the diameter of axial corallites. Histological analyses showed that the onset of gamete production/maturation occurred from June onwards. Most of the other Acropora species spawned from late May to early June. A. florida, which spawned in May/June, initiated gamete production in early April. We assumed that the two morphotypes of A. divaricata were reproductively isolated from most of the other Acropora species because of differences in the spawning seasons. We found that the spawning seasons of the two morphotypes slightly overlapped in 2015 but not in 2019, and inter-morphotype gamete compatibility was high. However, population genetics analyses and a phylogeny of the mitochondrial d-loop region showed that they were genetically distinct and rarely hybridized. Thus, the broadcast-spawning coral A. divaricata might have speciated when there might have been only a low possibility of interspecific gamete interaction.

Transcriptome characterization of BPG axis and expression profiles of ovarian steroidogenesis-related genes in the Japanese sardine

BackgroundThe clupeoid fishes are ecologically and commercially important fish species worldwide that exhibit a high level of population fluctuation, accompanied by alteration of reproductive traits. However, knowledge about their reproductive physiology in order to understand mechanisms underlying such population dynamics is limited. The endocrine system along with the brain–pituitary–gonadal (BPG) axis is critical for regulating reproduction. The aims of this study were to provide transcript data and genes related to the BPG axis, and to characterize the expression profiles of ovarian steroidogenesis-related genes in the Japanese sardine (Sardinops melanostictus, Clupeidae).ResultsRNA sequencing was performed using the sardine brain, pituitary, and gonad in both sexes. A total of 290,119 contigs were obtained and 115,173 non-redundant ORFs were annotated. The genes differentially expressed between ovary and testis were strongly associated with GO terms related to gamete production. The tissue-specific profile of the abundance of transcripts was characterized for the major regulators in the BPG axis, such as gonadotropin-releasing hormone, gonadotropin, and steroidogenic enzyme. By comparing between ovary and testis, out of eight different 17β-hydroxysteroid dehydrogenase (Hsd17b) genes identified, higher hsd17b7 expression was found in testis, whereas higher expression of hsd17b8, hsd17b10, hsd17b12a, and hsd17b12b was found in ovary. The cDNAs encoding key endocrine factors in the ovarian steroidogenic pathway were cloned, sequenced, and quantitatively assayed. In the pituitary, follicle-stimulating hormone beta peaked during vitellogenesis, while luteinizing hormone beta peaked at the completion of vitellogenesis. In the ovary, follicle-stimulating hormone receptor and luteinizing hormone receptor were upregulated from mid- to late phase of vitellogenesis. Furthermore, three steroidogenic enzyme genes (cyp11a1, cyp17a1, and cyp19a1a) gradually increased their expression during ovarian development, accompanying a rise in serum estradiol-17β, while 3β-hydroxysteroid dehydrogenase and steroidogenic acute regulatory protein did not change significantly.ConclusionsThis is the first report of deep RNA sequencing analysis of Japanese sardine, in which many key genes involved in the BPG axis were identified. Expression profiles of ovarian steroidogenesis-related genes provide a molecular basis of the physiological processes underlying ovarian development in the sardine. Our study will be a valuable resource for clarifying the molecular biology of clupeoid fishes.

Endogenous retroviruses drive species-specific germline transcriptomes in mammals.

Gene regulation in the germline ensures the production of high-quality gametes, long-term maintenance of the species, and speciation. Male germline transcriptomes undergo dynamic changes after the mitosis-to-meiosis transition and have been subject to evolutionary divergence among mammals. However, the mechanisms underlying germline regulatory divergence remain undetermined. Here, we show that endogenous retroviruses (ERVs) influence species-specific germline transcriptomes. After the mitosis-to-meiosis transition in male mice, specific ERVs function as active enhancers to drive germline genes, including a mouse-specific gene set, and bear binding motifs for critical regulators of spermatogenesis such as A-MYB. This raises the possibility that a genome-wide transposition of ERVs rewired germline gene expression in a species-specific manner. Of note, independently evolved ERVs are associated with the expression of human-specific germline genes, demonstrating the prevalence of ERV-driven mechanisms in mammals. Together, we propose that ERVs fine-tune species-specific transcriptomes in the mammalian germline.

The appraisal of body content (ABC) trial: obesity does not significantly impact gamete production in infertile men and women.

As obesity becomes increasingly prevalent, its impact on fertility has been a subject of great debate. Nearly all prior research is retrospective and evaluates obesity utilizing body mass index (BMI), which may overestimate adiposity in individuals with a greater amount of lean muscle and underestimate adiposity in those with less muscle mass. We prospectively evaluated 2013 couples undergoing infertility treatment with in vitro fertilization (IVF). Percent body fat (%BF) was measured by use of a bioelectric impedance analysis (BIA) scale at baseline. BMI was also determined. Ovarian reserve parameters, ovarian response to controlled ovarian hyperstimulation, and semen analyses were measured in correlation with their %BF and BMI. Females classified as obese based on %BF or BMI had lower serum FSH. However, when the analysis was limited to women without PCOS (n = 1706), obesity based on %BF or BMI was associated with lower serum AMH. Female obesity-regardless of a PCOS diagnosis-did not affect number of mature oocytes retrieved. Males who were in obese %BF category were found to have lower TMSC compared with normal weight counterparts (p < 0.05); however, the observed decrease was not significant enough to limit the success of assisted reproductive technologies. These findings suggest that while obesity may affect ovarian reserve in women variably depending on presence of PCOS, it does not affect number of mature oocytes available after COH. Similarly, while a high %BF in males is associated with lower TMSC, the observed difference is unlikely to affect IVF outcomes.

Assessment of Yangtze sturgeon as recipient for the production of American paddlefish gametes through spermatogonia transplantation

The Chinese paddlefish (Psephurus gladius), one of the world’s largest freshwater fish, was last seen alive in 2003; they are presumed now to be extinct. In fish, germ cell transplantation is currently known as one of the most powerful assisted reproductive technologies for the conservation of endangered species. In the event that a Chinese paddlefish is unexpectedly caught in the near future, we aimed to develop an experimental strategy to produce paddlefish gametes in the gonads of surrogate sturgeon. Spermatogonia were collected from the testes of 2.5-year-old immature male American paddlefish (Polyodon spathula), the species most closely related to the Chinese paddlefish, by Percoll gradient centrifugation, and transplanted into the peritoneal cavity of Yangtze sturgeon (Acipenser dabryanus) larvae at 7–8 days post-hatch. At two months post-transplantation, donor-derived spermatogonia had efficiently colonized in the recipient gonads and proliferated. A PCR analysis developed to detect xenogenic donor-derived mtDNA sequences in recipient gonads revealed that American paddlefish germ cells survived for at least seven months after transplantation in the gonads of Yangtze sturgeon recipients. These results show that the somatic microenvironment of Yangtze sturgeon gonads was able to support the colonization, proliferation, and survival of xenogeneic germ cells from a different taxonomic family. This study provides key information that could lead to future restoration of Chinese paddlefish using germ cell transplantation.

Do female frogs have higher resting metabolic rates than males? A case study with Xenopus allofraseri

AbstractThe energetic costs of body maintenance can have a profound influence on the energy that an individual can allocate to other functions such as growth, locomotion, or reproduction. Therefore, resting metabolism can ultimately affect an individual's survival or reproductive success, especially when food is limited. Although males and females often differ in their body composition (e.g. sex organs and fat accumulation) and body size, the occurrence and direction of sexual dimorphism in resting metabolism remains poorly understood in anurans. In the present study, we investigated whether males and females of the false Fraser's clawed frog Xenopus allofraseri differ in their resting metabolic rates. We used an open‐flow push‐through respirometry system to measure the volume of carbon dioxide (VCO2) produced by animals at rest. Variation inwas explained by ambient temperature, body size, and sex. For a similar body size, our results revealed that females had about a 50% higher resting metabolic rate (RMR) than males. We suggest that the enhanced investment in gamete production in females compared to males may explain this difference. We further suggest that a lower RMR in males compared to females at similar body size could be selectively advantageous as unallocated energy may be devoted to costly mating, in support of the ‘compensation’ hypothesis.

Parthenogenesis as a Solution to Hybrid Sterility: The Mechanistic Basis of Meiotic Distortions in Clonal and Sterile Hybrids.

Hybrid sterility is a hallmark of speciation, but the underlying molecular mechanisms remain poorly understood. Here, we report that speciation may regularly proceed through a stage at which gene flow is completely interrupted, but hybrid sterility occurs only in male hybrids whereas female hybrids reproduce asexually. We analyzed gametogenic pathways in hybrids between the fish species Cobitis elongatoides and C. taenia, and revealed that male hybrids were sterile owing to extensive asynapsis and crossover reduction among heterospecific chromosomal pairs in their gametes, which was subsequently followed by apoptosis. We found that polyploidization allowed pairing between homologous chromosomes and therefore partially rescued the bivalent formation and crossover rates in triploid hybrid males. However, it was not sufficient to overcome sterility. In contrast, both diploid and triploid hybrid females exhibited premeiotic genome endoreplication, thereby ensuring proper bivalent formation between identical chromosomal copies. This endoreplication ultimately restored female fertility but it simultaneously resulted in the obligate production of clonal gametes, preventing any interspecific gene flow. In conclusion, we demonstrate that the emergence of asexuality can remedy hybrid sterility in a sex-specific manner and contributes to the speciation process.

Single-cell RNA sequencing reveals the landscape of early female germ cell development.

Meiosis initiation is a crucial step for the production of haploid gametes, which occurs from anterior to posterior in fetal ovaries. The asynchrony of the transition from mitosis to meiosis results in heterogeneity in the female germ cell populations, which limits the studies of meiosis initiation and progression at a higher resolution level. To dissect the process of meiosis initiation, we investigated the transcriptional profiles of 19363 single germ cells collected from E12.5, E14.5, and E16.5 mouse fetal ovaries. Clustering analysis identified seven groups and defined dozens of corresponding transcription factors, providing a global view of cellular differentiation from primordial germ cells toward meiocytes. Furthermore, we explored the dynamics of gene expression within the developmental trajectory with special focus on the critical state of meiosis. We found that meiosis initiation occurs as early as E12.5 and the cluster of oogonia_4 is the critical state between mitosis and meiosis. Our data provide key insights into the transcriptome features of peri-meiotic female germ cells, which offers new information not only on meiosis initiation and progression but also on screening pathogenic mutations in meiosis-associated diseases.