Two-directional trafficking of the IFT25 protein in the developing mouse sperm flagella.

IF 3.1 2区 生物学 Q2 REPRODUCTIVE BIOLOGY
Wei Li, Changmin Niu, Yi Tian Yap, Tao Li, Cheng Zheng, Mariska Goswami, Sanjana Kandiraju, Opeyemi Dhikhirullahi, Jie Xu, Jifeng Zhang, Christopher V Kelly, Zhibing Zhang
{"title":"Two-directional trafficking of the IFT25 protein in the developing mouse sperm flagella.","authors":"Wei Li, Changmin Niu, Yi Tian Yap, Tao Li, Cheng Zheng, Mariska Goswami, Sanjana Kandiraju, Opeyemi Dhikhirullahi, Jie Xu, Jifeng Zhang, Christopher V Kelly, Zhibing Zhang","doi":"10.1093/biolre/ioae171","DOIUrl":null,"url":null,"abstract":"<p><p>Intraflagellar transport 25 (IFT25) is a component of the IFT-B complex. In mice, even though this IFT component is not required for cilia formation in somatic cells, it is essential for sperm formation. However, the intracellular localization of this protein in male germ cells is not known given no reliable antibodies are available for histologic studies, and the dynamic trafficking in the developing sperm flagella is not clear. To examine localization of the protein in male germ cells and further investigate the mechanism of IFT in sperm formation, particularly to look into the dynamic trafficking of the protein, we generated a mouse IFT25-GFP knock-in (KI) mouse model using the CRISPR/cas9 system, with the mouse IFT25 protein fused with a GFP tag in the C-terminus. Three independent lines were analyzed. Western blotting using both anti-IFT25 and anti-GFP antibodies showed that the IFT25-GFP fusion protein was highly abundant only in the testis, which is consistent with the endogenous IFT25 protein. Examination of localization of the IFT25-GFP in isolated germ cells revealed that the fusion protein was present in the cytoplasm of spermatocytes and round spermatids and a strong signal was present in the developing sperm flagellar. The homozygous KI mice had normal spermatogenesis, fertility and sperm parameters. Diffusion analysis of IFT25 within the developing flagellar revealed the presence of both mobile and immobile fractions as revealed by fluorescence recovery after photobleaching (FRAP). Kymograph and FRAP analyses demonstrate the transport of IFT25-GFP within the developing tail demonstrate no apparent preference for trafficking towards and away from the cell body. The speed of trafficking depends on the stage of sperm development, ranging from highly mobile unrestricted diffusion initially, mobile punctate structures in developing sperm, and immobile punctate structures in mature sperm. Our studies demonstrate that mouse IFT25 travels along the developing sperm flagella in two directions that might be essential for functional sperm formation.</p>","PeriodicalId":8965,"journal":{"name":"Biology of Reproduction","volume":" ","pages":""},"PeriodicalIF":3.1000,"publicationDate":"2024-11-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biology of Reproduction","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1093/biolre/ioae171","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"REPRODUCTIVE BIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Intraflagellar transport 25 (IFT25) is a component of the IFT-B complex. In mice, even though this IFT component is not required for cilia formation in somatic cells, it is essential for sperm formation. However, the intracellular localization of this protein in male germ cells is not known given no reliable antibodies are available for histologic studies, and the dynamic trafficking in the developing sperm flagella is not clear. To examine localization of the protein in male germ cells and further investigate the mechanism of IFT in sperm formation, particularly to look into the dynamic trafficking of the protein, we generated a mouse IFT25-GFP knock-in (KI) mouse model using the CRISPR/cas9 system, with the mouse IFT25 protein fused with a GFP tag in the C-terminus. Three independent lines were analyzed. Western blotting using both anti-IFT25 and anti-GFP antibodies showed that the IFT25-GFP fusion protein was highly abundant only in the testis, which is consistent with the endogenous IFT25 protein. Examination of localization of the IFT25-GFP in isolated germ cells revealed that the fusion protein was present in the cytoplasm of spermatocytes and round spermatids and a strong signal was present in the developing sperm flagellar. The homozygous KI mice had normal spermatogenesis, fertility and sperm parameters. Diffusion analysis of IFT25 within the developing flagellar revealed the presence of both mobile and immobile fractions as revealed by fluorescence recovery after photobleaching (FRAP). Kymograph and FRAP analyses demonstrate the transport of IFT25-GFP within the developing tail demonstrate no apparent preference for trafficking towards and away from the cell body. The speed of trafficking depends on the stage of sperm development, ranging from highly mobile unrestricted diffusion initially, mobile punctate structures in developing sperm, and immobile punctate structures in mature sperm. Our studies demonstrate that mouse IFT25 travels along the developing sperm flagella in two directions that might be essential for functional sperm formation.

发育中小鼠精子鞭毛中 IFT25 蛋白的双向运输
纤毛内运输 25(IFT25)是 IFT-B 复合物的一个组成部分。在小鼠体内,尽管体细胞纤毛的形成不需要这种 IFT 成分,但精子的形成却离不开它。然而,由于没有可靠的抗体可用于组织学研究,该蛋白在雄性生殖细胞中的胞内定位尚不清楚,发育中精子鞭毛的动态运输也不明确。为了研究该蛋白在雄性生精细胞中的定位,并进一步研究 IFT 在精子形成中的作用机制,尤其是研究该蛋白的动态运输,我们利用 CRISPR/cas9 系统生成了小鼠 IFT25-GFP 基因敲入(KI)小鼠模型,小鼠 IFT25 蛋白的 C 端融合了一个 GFP 标记。对三个独立品系进行了分析。使用抗 IFT25 和抗 GFP 抗体进行的 Western 印迹显示,IFT25-GFP 融合蛋白仅在睾丸中含量较高,这与内源性 IFT25 蛋白一致。对 IFT25-GFP 在离体生殖细胞中的定位研究发现,该融合蛋白存在于精母细胞和圆形精子的细胞质中,在发育中的精子鞭毛中存在一个强信号。同源 KI 小鼠的精子发生、生育能力和精子参数正常。通过光漂白后荧光恢复(FRAP)对发育中鞭毛内的 IFT25 进行扩散分析,发现其中既有移动的部分,也有不移动的部分。Kymograph和FRAP分析表明,IFT25-GFP在发育中的尾部内的迁移没有明显的向细胞体或远离细胞体的迁移偏好。运输速度取决于精子的发育阶段,从最初的高流动性无限制扩散,到发育中精子的流动性点状结构,再到成熟精子的不流动性点状结构。我们的研究表明,小鼠 IFT25 沿着发育中精子鞭毛的两个方向移动,这可能是功能性精子形成所必需的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Biology of Reproduction
Biology of Reproduction 生物-生殖生物学
CiteScore
6.30
自引率
5.60%
发文量
214
审稿时长
1 months
期刊介绍: Biology of Reproduction (BOR) is the official journal of the Society for the Study of Reproduction and publishes original research on a broad range of topics in the field of reproductive biology, as well as reviews on topics of current importance or controversy. BOR is consistently one of the most highly cited journals publishing original research in the field of reproductive biology.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信