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The role of MEIOC at the transition from mitosis to meiosis during mammalian spermatogenesis

ABSTRACT: The role of MEIOC at the transition from mitosis to meiosis during mammalian spermatogenesis

PROVIDER: PRJNA962497 | ENA |

REPOSITORIES: ENA

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			Action	DRS
	SRR24323021.fastq.gz	Fastqsanger.gz
	SRR24323022.fastq.gz	Fastqsanger.gz
	SRR24323023.fastq.gz	Fastqsanger.gz
	SRR24323024.fastq.gz	Fastqsanger.gz
	SRR24323025.fastq.gz	Fastqsanger.gz

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The role of MEIOC at the transition from mitosis to meiosis during mammalian spermatogenesis [bulkRNAseq]

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The role of MEIOC at the transition from mitosis to meiosis during mammalian spermatogenesis [scRNA]

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The role of MEIOC at the transition from mitosis to meiosis during mammalian spermatogenesis [bulkRNAseq]

Project description:The role of MEIOC at the transition from mitosis to meiosis during mammalian spermatogenesis [bulkRNAseq]

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Project description:The role of MEIOC at the transition from mitosis to meiosis during mammalian spermatogenesis [scRNA]

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Poised chromatin and bivalent domains facilitate the mitosis-to-meiosis transition in the male germline

Project description:The male germline transcriptome changes dramatically during the mitosis-to-meiosis transition to activate late spermatogenesis genes and to transiently suppress genes commonly expressed in somatic lineages and spermatogenesis progenitor cells, termed somatic/progenitor genes. These changes reflect epigenetic regulation. Induction of late spermatogenesis genes during spermatogenesis is facilitated by poised chromatin established in the stem cell phases of spermatogonia, whereas silencing of somatic/progenitor genes during meiosis and postmeiosis is associated with formation of bivalent domains which also allows the recovery of the somatic/progenitor program after fertilization. Importantly, during spermatogenesis mechanisms of epigenetic regulation on sex chromosomes are different from autosomes: X-linked somatic/progenitor genes are suppressed by meiotic sex chromosome inactivation without deposition of H3K27me3. Our results suggest that bivalent H3K27me3 and H3K4me2/3 domains are not limited to developmental promoters (which maintain bivalent domains that are silent throughout the reproductive cycle), but also underlie reversible silencing of somatic/progenitor genes during the mitosis-to-meiosis transition in late spermatogenesis. 29 samples analyzed by ChIP-Seq

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Poised chromatin and bivalent domains facilitate the mitosis-to-meiosis transition in the male germline

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Project description:Spermatocyte meiosis is the cornerstone of mammalian production. Thousands of long noncoding RNAs (lncRNAs) have been reported to be functional in various cellular processes, but the function of lncRNAs in meiosis remains largely unknown. Here, we profiled lncRNAs in spermatocytes at stage I of meiosis and identified a testis-specific lncRNA, Rbakdn, as a vital regulator of meiosis. Rbakdn is dynamically expressed during meiosis I, and Rbakdn knockdown inhibits meiosis in vitro. Furthermore, Rbakdn knockdown in testes in mice by intratesticular injection disturbs meiosis, reduces testicular volume, and increases apoptosis of spermatocytes, resulting in vacuolation of the seminiferous tubules. Rbakdn can bind to Ptbp2, an RNA-binding protein that is important in the regulation of the alternative splicing of many genes in spermatogenesis. Rbakdn knockdown leads to a decrease in Ptbp2 through the ubiquitination degradation pathway, indicating that Rbakdn maintains the stability of Ptbp2. In conclusion, our study identified an lncRNA, Rbakdn, with a crucial role in meiosis.

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Project description:Male germ cell meiosis is essential for generating haploid spermatozoa in mice. Here, we investigate the essential role of DIS3 in male germ cell meiosis in mice. Conditional inactivation of DIS3 in spermatocytes with Stra8-cre transgenic mice have severely impaired meiotic progression, which results in defective meiosis and spermatogenesis. RNA-seq analysis reveals that Dis3 deficiency causes significant dysregulation of the expression of transcripts in mutant testes. Meiosis-associated genes are significantly decreased in the absence of DIS3. Therefore, we show that DIS3 ribonuclease plays a critical role in germ cell meiosis during spermatogenesis in mice.

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