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Piwi信号通路改变导致隐睾症中LINE-1转座子去抑制和不育症发展。

Piwi-pathway alteration induces LINE-1 transposon derepression and infertility development in cryptorchidism.

作者信息

Hadziselimovic Faruk, Hadziselimovic Nils O, Demougin Philippe, Krey Gunthild, Oakeley Eduard

机构信息

Institute for Andrology, Liestal, Switzerland.

出版信息

Sex Dev. 2015;9(2):98-104. doi: 10.1159/000375351. Epub 2015 Mar 13.

DOI:10.1159/000375351
PMID:25791297
Abstract

Spermatogonia contain processing bodies that harbor P-element-induced wimpy testis (Piwi) proteins. Piwi proteins are associated specifically with Piwi-interacting RNAs to silence transposable DNA elements. Loss-of-function mutations in the Piwi pathway lead to derepression of transposable elements, resulting in defective spermatogenesis. Furthermore, deletion of gametocyte-specific factor 1 (GTSF1), a factor involved in Piwi-mediated transcriptional repression, causes male-specific sterility and derepression of LINE-1 (L1) retrotransposons. No previous studies have examined GTSF1, L1 and PIWIL4 expression in cryptorchidism. We examined transposon-silencing genes and L1 transposon expression in testicular biopsies with Affymetrix microarrays and immunohistology. Seven members of the Tudor gene family, 3 members of the DEAD-box RNA helicase family, and the GTSF1 gene were found to show significantly lower RNA signals in the high-infertility-risk group. In the immunohistochemical analysis, patients from the low-infertility-risk group showed coherently stronger staining for GTSF1 and PIWIL4 proteins and weaker staining for L1 transposon when compared to the high-infertility-risk samples. These new findings provide first evidence consistent with the idea that infertility in cryptorchidism is a consequence of alterations in the Piwi pathway and transposon derepression induced by the impaired function of mini-puberty.

摘要

精原细胞含有携带P元件诱导的弱精睾丸(Piwi)蛋白的加工小体。Piwi蛋白与Piwi相互作用RNA特异性结合,以沉默转座DNA元件。Piwi通路中的功能丧失突变导致转座元件去抑制,从而导致精子发生缺陷。此外,配子细胞特异性因子1(GTSF1)的缺失,一种参与Piwi介导的转录抑制的因子,会导致雄性特异性不育和LINE-1(L1)逆转座子的去抑制。以前没有研究检查过隐睾症中GTSF1、L1和PIWIL4的表达。我们用Affymetrix微阵列和免疫组织学方法检测了睾丸活检组织中转座子沉默基因和L1转座子的表达。发现Tudor基因家族的7个成员、DEAD盒RNA解旋酶家族 的3个成员以及GTSF1基因在高不孕风险组中显示出明显较低的RNA信号。在免疫组织化学分析中,与高不孕风险样本相比,低不孕风险组的患者GTSF1和PIWIL4蛋白染色一致更强,而L1转座子染色更弱。这些新发现首次提供了证据,支持隐睾症中的不育是Piwi通路改变和小青春期功能受损诱导的转座子去抑制的结果这一观点。

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Piwi-pathway alteration induces LINE-1 transposon derepression and infertility development in cryptorchidism.Piwi信号通路改变导致隐睾症中LINE-1转座子去抑制和不育症发展。
Sex Dev. 2015;9(2):98-104. doi: 10.1159/000375351. Epub 2015 Mar 13.
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