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首页> 外文期刊>Molecular human reproduction. >Identification of genes expressed in human primordial germ cells at the time of entry of the female germ line into meiosis.
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Identification of genes expressed in human primordial germ cells at the time of entry of the female germ line into meiosis.

机译:鉴定女性生殖系减数分裂进入人类原始生殖细胞中表达的基因。

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In mammals, primordial germ cells (PGCs) are first observed in the extraembryonic mesoderm from where they migrate through the hindgut and its mesentery to the genital ridge to colonize the developing gonads. Soon after reaching the gonads, the female PGCs enter meiosis, while the male PGCs are arrested in mitosis and enter meiosis postnatally. To gain an insight into the molecular events controlling human germ cell development, we determined specific profiles of gene expression using cDNA prepared from PGCs isolated from male and female fetal gonads at 10 weeks gestation, when female PGCs start to enter meiosis. The identity of the isolated PGCs, and the cDNA molecules prepared from them, was confirmed respectively, by alkaline phosphatase staining and by the presence of transcripts of OCT4, a marker gene for PGCs and pluripotent stem cells in mice. Using differential display to compare the profiles of gene expression of male and female germ cells with each other and with that of a whole 10 week old fetus, we have identified eight transcripts differentially expressed in male and/or female germ cells. Among these transcripts, we have identified a member of the olfactory receptor gene family, which contains genes known to be germline-specific in the dog and possibly associated with chemotactic function. Another transcript is common to a previously isolated sequence from the human testis and we have extended this sequence towards the 5' end for partial characterization. The germline-specific sequences also include two novel sequences not represented in the databases. These findings are highly encouraging for the elucidation of the genetic programming of male and female germ line development.
机译:在哺乳动物中,首先在胚外中胚层中观察到原始生殖细胞(PGC),从那里它们通过后肠及其肠系膜迁移到生殖器ridge中,从而定居发育中的性腺。到达性腺后不久,雌性PGC进入减数分裂,而雄性PGC被捕入有丝分裂并在出生后进入减数分裂。为了深入了解控制人类生殖细胞发育的分子事件,我们使用了从妊娠10周时从雌性和雄性胎儿性腺中分离的PGC制备的cDNA(当女性PGC开始进入减数分裂时)确定的特定基因表达谱。通过碱性磷酸酶染色和小鼠中PGC和多能干细胞的标记基因OCT4的转录本的存在,分别证实了分离出的PGC和由其制备的cDNA分子的身份。使用差异显示来比较男性和女性生殖细胞的基因表达谱以及与整个10周大胎儿的基因表达谱,我们已经鉴定出在男性和/或女性生殖细胞中差异表达的8个转录本。在这些成绩单中,我们已经确定了嗅觉受体基因家族的成员,该家族包含已知在狗中具有种系特异性并且可能与趋化功能相关的基因。另一个转录本是先前从人类睾丸中分离出的序列所共有的,我们已将该序列扩展至5'端以进行部分表征。种系特异性序列还包括数据库中未显示的两个新序列。这些发现为阐明男性和女性种系发育的遗传程序提供了极大的鼓舞。

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