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DNAH7 功能丧失性突变导致男性不育,与人类精子鞭毛和线粒体异常有关。

Loss of function mutation in DNAH7 induces male infertility associated with abnormalities of the sperm flagella and mitochondria in human.

机构信息

Department of Obstetrics and Gynecology, The First Affiliated Hospital of Anhui Medical University, Hefei, Anhui, China.

NHC Key Laboratory of Study on Abnormal Gametes and Reproductive Tract, Anhui Medical University, Hefei, Anhui, China.

出版信息

Clin Genet. 2022 Aug;102(2):130-135. doi: 10.1111/cge.14146. Epub 2022 May 17.

Abstract

Male infertility is an increasingly serious health problem affecting couples of reproductive age. Mutations in axoneme-associated genes cause male infertility. Dynein arm proteins are essential in sustaining normal axonemes and promote flagellar motility. However, the function of DNAH7 in male fertility in vivo remains unclear. Herein, we showed that DNAH7 disruption in humans results in male infertility, which was characterised by multiple morphological abnormalities of sperm flagella. The axoneme structure of the sperm from a DNAH7-deficient patient revealed the loss of inner dynein arms. Moreover, the mitochondria of the sperm flagella detached and dispersed outside the axoneme, leading to abnormalities in the mitochondrial sheath in the mid-piece region. Live birth was achieved via intracytoplasmic sperm injection. Thus, DNAH7 is critical for axoneme and mitochondrial development in human sperm. These findings further clarify the spectrum of DNAH7 biology and provide new insights for diagnosing infertility and treating patients harbouring DNAH7 mutations.

摘要

男性不育是一个日益严重的健康问题,影响着育龄夫妇。轴丝相关基因的突变导致男性不育。动力蛋白臂蛋白对于维持正常的轴丝至关重要,并促进鞭毛运动。然而,DNAH7 在体内对男性生育力的功能仍不清楚。本文中,我们发现人类 DNAH7 的缺失会导致男性不育,其特征是精子鞭毛的多种形态异常。DNAH7 缺陷患者精子的轴丝结构显示内动力蛋白臂的缺失。此外,精子鞭毛的线粒体脱离并分散在轴丝外,导致中段线粒体鞘的异常。通过胞质内精子注射实现了活产。因此,DNAH7 对于人精子的轴丝和线粒体发育至关重要。这些发现进一步阐明了 DNAH7 的生物学范围,并为诊断不育症和治疗携带 DNAH7 突变的患者提供了新的见解。

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