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体内Fshr表达需要远端调控元件。

Distal regulatory elements are required for Fshr expression, in vivo.

作者信息

Hermann Brian P, Hornbaker Kaori I, Maran Rengasamy R M, Heckert Leslie L

机构信息

Department of Molecular and Integrative Physiology, University of Kansas Medical Center, 3901 Rainbow Boulevard, Kansas City, KS 66160, USA.

出版信息

Mol Cell Endocrinol. 2007 Jan 2;260-262:49-58. doi: 10.1016/j.mce.2006.01.017. Epub 2006 Nov 9.

Abstract

The gonadotropin follicle-stimulating hormone (FSH) is required for initiation and maintenance of normal gametogenesis and acts through a specific, cell-surface receptor (Fshr) present only on Sertoli and granulosa cells in the gonads. Despite extensive examination of the transcriptional mechanisms regulating Fshr, the sequences directing its expression to these cells remain unidentified. To establish the minimal region necessary for Fshr expression, we generated transgenic mice carrying a yeast artificial chromosome (YAC) that contained 413 kilobases (kb) of the rat Fshr locus (YAC60). Transgene expression, as determined by RT-PCR, was absent from immature testis and Sertoli cells, limited to germ cells of the adult testis, and never observed in the ovary. While the data is limited to only one transgenic line, it suggests that the 413kb region does not specify the normal spatiotemporal expression pattern of Fshr. Comparative genomics was used to identify potential distal regulatory elements, revealing seven regions of high evolutionary conservation (>80% identity over 100bp or more), six of which were absent from the transgene. Functional examination of the evolutionary conserved regions (ECRs) by transient transfection revealed that all of the ECRs had modest transcriptional activity in Sertoli or myoid cells with two, ECR4 and ECR5, showing differential effects in expressing and non-expressing cells. These data reveal that distal regulatory regions (outside the 413kb in YAC60) are required for appropriate temporal and spatial Fshr expression and implicate the identified ECRs in transcriptional regulation of Fshr.

摘要

促性腺激素卵泡刺激素(FSH)是启动和维持正常配子发生所必需的,它通过一种仅存在于性腺支持细胞和颗粒细胞表面的特异性细胞表面受体(Fshr)发挥作用。尽管对调节Fshr的转录机制进行了广泛研究,但将其表达导向这些细胞的序列仍未确定。为了确定Fshr表达所需的最小区域,我们构建了携带酵母人工染色体(YAC)的转基因小鼠,该YAC包含413千碱基(kb)的大鼠Fshr基因座(YAC60)。通过RT-PCR测定,转基因表达在未成熟睾丸和支持细胞中缺失,仅限于成年睾丸的生殖细胞,在卵巢中从未观察到。虽然数据仅限于一个转基因品系,但这表明413kb区域并未指定Fshr的正常时空表达模式。利用比较基因组学来识别潜在的远端调控元件,发现了七个高度进化保守的区域(在100bp或更长区域内同一性>80%),其中六个区域在转基因中不存在。通过瞬时转染对进化保守区域(ECRs)进行功能检测,发现所有ECRs在支持细胞或肌样细胞中都具有适度的转录活性,其中ECR4和ECR5在表达和不表达细胞中表现出不同的效应。这些数据表明,远端调控区域(YAC60中413kb以外)是Fshr正常时空表达所必需的,并表明所鉴定的ECRs参与了Fshr的转录调控。

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