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SLC35G3是一种用于精子糖蛋白形成的UDP-N-乙酰葡糖胺转运蛋白,是小鼠雄性生育能力的基础。

SLC35G3 is a UDP-N-acetylglucosamine transporter for sperm glycoprotein formation and underpins male fertility in mice.

作者信息

Mashiko Daisuke, Tonai Shingo, Miyata Haruhiko, Matzuk Martin M, Ikawa Masahito

机构信息

Department of Experimental Genome Research, Research Institute for Microbial Diseases, Osaka University, Suita, Osaka 565-0871, Japan.

Immunology Frontier Research Center, Osaka University, Suita, Osaka 565-0871, Japan.

出版信息

bioRxiv. 2025 May 15:2025.05.12.653469. doi: 10.1101/2025.05.12.653469.

Abstract

Despite the recognized importance of glycans in biological phenomena, their complex roles in spermatogenesis and sperm function remain unclear. SLC35G3, a 10-transmembrane protein specifically found in early round spermatids, belongs to the sugar-nucleotide transporter family, indicating its involvement in glycan formation. In this study, we found that knockout male mice were sterile due to impaired sperm functions in uterotubal junction passage, zona pellucida binding, and oocyte fusion. Mouse SLC35G3 has UDP-GlcNAc transporter activity, and its ablation caused abnormal processing of the sperm plasma membrane and acrosome membrane proteins. Reported human mutations (F267L and T179HfsTer27) diminished the UDP-GlcNAc transporter activity of SLC35G3, implying infertility risks in males carrying these mutations. Our findings unveil the vital roles of SLC35G3 in the glycan formation of sperm membrane proteins critical for sperm fertilizing ability.

摘要

尽管聚糖在生物学现象中的重要性已得到认可,但其在精子发生和精子功能中的复杂作用仍不清楚。SLC35G3是一种在早期圆形精子细胞中特异性发现的10次跨膜蛋白,属于糖核苷酸转运蛋白家族,表明它参与聚糖形成。在本研究中,我们发现基因敲除的雄性小鼠不育,原因是在子宫输卵管连接处通过、透明带结合和卵母细胞融合过程中精子功能受损。小鼠SLC35G3具有UDP-GlcNAc转运活性,其缺失导致精子质膜和顶体膜蛋白的加工异常。报道的人类突变(F267L和T179HfsTer27)降低了SLC35G3的UDP-GlcNAc转运活性,这意味着携带这些突变的男性存在不育风险。我们的研究结果揭示了SLC35G3在对精子受精能力至关重要的精子膜蛋白聚糖形成中的重要作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a5a5/12132321/b34963ddae60/nihpp-2025.05.12.653469v1-f0001.jpg

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