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一种在大鼠睾丸和附睾中表达的雄激素调节的同源盒基因。

An androgen-regulated homeobox gene expressed in rat testis and epididymis.

作者信息

Lindsey J S, Wilkinson M F

机构信息

Molecular Microbiology and Immunology Graduate Program, Oregon Health Sciences University, Portland 97201, USA.

出版信息

Biol Reprod. 1996 Nov;55(5):975-83. doi: 10.1095/biolreprod55.5.975.

Abstract

Homeobox genes encode DNA-binding proteins that regulate the transcription of subordinate downstream genes. In this study, we show that the Pem homeobox gene is expressed and regulated in a unique manner in neonatal and adult rats. Pem gene expression was primarily confined to reproductive tissue: epididymis, testis, ovary, and placenta. In the epididymis, Pem transcripts were localized by in situ hybridization analysis to the proximal cauda region, a site where spermatozoa gain fertilization competence. Pem mRNA levels dramatically increased between Days 21 and 26 postpartum in the epididymis, coincident with the induction of genes known to be responsive to testosterone (T), but in contrast to that of other genes examined, including the Hoxc-8 homeobox gene. Pem expression was shown to be T-dependent on the basis of an absence of Pem transcripts in the epididymides of hypophysectomized rats and restoration of normal Pem mRNA levels after administration of T. In the testis, Pem mRNA levels were elevated earlier (between Days 12 and 15 postpartum) and less dramatically than in epididymis. Pem gene expression in the testis was depressed after hypophysectomy, but normal levels of Pem expression were not restored by T treatment under the same conditions that permitted normal Pem expression in the epididymis. To our knowledge Pem is the first reported putative transcription factor that has been demonstrated to depend on androgens for expression in the epididymis, and thus Pem is a candidate as a regulator of androgen-dependent events in this tissue.

摘要

同源框基因编码调控下游从属基因转录的DNA结合蛋白。在本研究中,我们发现Pem同源框基因在新生和成年大鼠中以独特的方式表达和调控。Pem基因表达主要局限于生殖组织:附睾、睾丸、卵巢和胎盘。在附睾中,通过原位杂交分析将Pem转录本定位到附睾尾近端区域,这是精子获得受精能力的部位。附睾中Pem mRNA水平在产后第21天至26天之间显著增加,这与已知对睾酮(T)有反应的基因的诱导相一致,但与包括Hoxc - 8同源框基因在内的其他检测基因不同。基于垂体切除大鼠附睾中不存在Pem转录本以及给予T后恢复正常Pem mRNA水平,表明Pem表达依赖于T。在睾丸中,Pem mRNA水平升高的时间更早(产后第12天至15天之间),且升高幅度小于附睾。垂体切除后睾丸中的Pem基因表达降低,但在允许附睾中Pem正常表达的相同条件下,T处理并未恢复Pem的正常表达水平。据我们所知,Pem是首个被证明在附睾中表达依赖雄激素的推定转录因子,因此Pem是该组织中雄激素依赖性事件调节因子的候选者。

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