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Deficiency of the transcription factor PLAG1 results in aberrant coiling and morphology of the epididymis

机译:转录因子Plag1的缺乏导致异形骨折的异常卷曲和形态

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摘要

Mice deficient in the transcription factor pleomorphic adenoma gene 1 (PLAG1) exhibit reproductive issues that are characterized, in part, by decreased progressive sperm motility in the male. However, the underlying cause of this impairment is unknown. As epididymal transit is critical for sperm maturation and motility, the morphology of the epididymis of -deficient mice was investigated and the spatial expression patterns of PLAG1 protein and mRNA were identified. Using X-gal staining and hybridization, PLAG1 was shown to be widely expressed in both the epithelium and stroma in all regions of the mouse epididymis. Interestingly, the X-gal staining pattern was markedly different in the cauda, where it could be suggestive of PLAG1 secretion into the epididymal lumen. At all ages investigated, the morphology of epididymides from knockout (KO) mice was aberrant; the tubule failed to elongate and coil, particularly in the corpus and cauda, and the cauda was malformed, lacking its usual bulbous shape. Moreover, the epididymides from KO mice were significantly reduced in size relative to body weight. In 20% of -deficient mice, the left testicle and epididymis were lacking. The impaired morphogenesis of the epididymal tubule is likely to be a major contributing factor to the fertility problems observed in male -deficient mice. These results also establish PLAG1 as an important regulator of male reproduction, not only through its involvement in testicular sperm production, but also via its role in the development and function of the epididymis.
机译:缺乏转录因子的脑梗死腺瘤基因1(PLAG1)的小鼠表现出具有特征的生殖问题,部分地通过降低雄性的逐步精子运动。然而,这种损害的潜在原因是未知的。由于附睾转运对于精子成熟和动力至关重要,研究了缺料小鼠的附睾的形态,并鉴定了Plag1蛋白和mRNA的空间表达模式。使用X-GAL染色和杂交,显示PLAG1在小鼠附睾的所有区域中的上皮和基质中广泛表达。有趣的是,X-gal染色模式在Cauda中显着不同,在那里它可以提示Plag1分泌到附睾内腔中。在调查的所有年龄,来自敲除(KO)小鼠的附睾形态是异常的;小管未能细长,卷材,特别是在胼cou,并且粗毛畸形,缺乏常规的球形形状。此外,来自KO小鼠的附睾明显减小相对于体重。在20%的缺血小鼠中,缺乏左睾丸和附睾。附睾小管的损害的形态发生可能是男性缺陷小鼠中观察到的生育问题的主要贡献因素。这些结果还建立了Plag1作为男性繁殖的重要调节因子,而不仅仅是通过其参与睾丸精子产生,而且通过其在附睾的发挥作用中的作用。

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