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克兰费尔特综合征男性患者中LDOC1基因的表达

LDOC1 Gene Expression in Men With Klinefelter Syndrome.

作者信息

Salemi Michele, Condorelli Rosita A, Longo Giusi, Bullara Valentina, Romano Carmelo, Campagna Cristina, Bosco Paolo, La Vignera Sandro, Calogero Aldo E

机构信息

Oasi Institute (IRCCS) for Research on Mental Retardation and Brain Aging, Troina, Italy.

Section of Endocrinology,Andrology and Internal Medicine, Department of Medical and Pediatric Sciences, University of Catania, Catania, Italy.

出版信息

J Clin Lab Anal. 2016 Sep;30(5):408-10. doi: 10.1002/jcla.21870. Epub 2016 Apr 13.

Abstract

Klinefelter syndrome (KS) results from an extra chromosome X, which is due to the failure of normal chromosomal segregation during meiosis. Patients with KS have gynecomastia, small testes, and azoospermia. Apoptosis is a mechanism responsible for the normal regulation of spermatogenesis. LDOC1 gene is a known regulator of nuclear factor mediated pathway to apoptosis through inhibition of nuclear factor kappa B (NF-kappaB). Furthermore, the transcription factor myeloid zinc finger gene 1 (MZF-1) has been shown to interact with LDOC1 and to enhance LDOC1 activity favoring apoptosis. We investigated the expression of LDOC1 gene mRNA, by quantitative reverse transcription polymerase chain reaction (qRT-PCR), in peripheral blood leukocytes of 13 patients with KS compared to 13 healthy men chosen as controls. LDOC1 expression was higher in 9 of the 13 KS patient compared to normal controls. These finding led us to hypothesize that LDOC1 gene upregulation may play a role in the spermatogenesis derangement observed in patients with KS.

摘要

克兰费尔特综合征(KS)是由额外的一条X染色体导致的,这是由于减数分裂过程中正常染色体分离失败所致。KS患者有男性乳腺增生、小睾丸和无精子症。细胞凋亡是一种负责精子发生正常调节的机制。LDOC1基因是一种已知的通过抑制核因子κB(NF-κB)来调节核因子介导的细胞凋亡途径的因子。此外,转录因子髓系锌指基因1(MZF-1)已被证明与LDOC1相互作用,并增强LDOC1促进细胞凋亡的活性。我们通过定量逆转录聚合酶链反应(qRT-PCR)研究了13例KS患者外周血白细胞中LDOC1基因mRNA的表达,并与13名作为对照的健康男性进行了比较。与正常对照相比,13例KS患者中有9例的LDOC1表达更高。这些发现使我们推测,LDOC1基因上调可能在KS患者精子发生紊乱中起作用。

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