GPI转氨酶复合体是斑马鱼原始生殖细胞迁移和发育所必需的。

IF 5.3 2区 生物学 Q2 CELL BIOLOGY Journal of Molecular Cell Biology Pub Date : 2024-12-31 DOI:10.1093/jmcb/mjae058
Weiying Zhang, Yaqi Li, Jing Chen, Likun Yao, Bingjie Zhang, Lin Zhang, Boqi Liu, Weimin Shen, Anming Meng, Xiaotong Wu
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引用次数: 0

摘要

当没有跨膜结构域的蛋白质通过GPI转氨酶(GPIT)复合物与糖基磷脂酰肌醇(GPI)分子共价连接时,可以锚定在细胞表面以调节各种生物过程。然而,对于GPIT复合物是否以及如何影响原始生殖细胞(PGC)的发育仍然知之甚少。在本研究中,我们报道了GPI转氨酶在斑马鱼胚胎PGC迁移和发育中的重要作用。pigu或pigk的突变,都编码必需的GPIT复合物亚基,导致PGC迁移缺陷,PGC位于异位,PGC计数减少。值得注意的是,对PGCs中丝足的详细分析显示,突变胚中丝足沿迁移方向分布的极性减弱。PGC移植和PGC特异性救援实验表明PGC和体细胞表达的Pigu都是PGC迁移所必需的。此外,在pigu突变体PGCs中,pgc特异性基因的表达水平随着体细胞基因的抑制而降低。因此,我们认为GPIT复合物在PGC迁移和发展过程中起着关键作用。
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GPI transamidase complex is required for primordial germ cell migration and development in zebrafish.

Proteins without transmembrane domains could be anchored to the cell surface for regulating various biological processes when covalently linked to glycosylphosphatidylinositol (GPI) molecules by the GPI transamidase (GPIT) complex. However, it remains poorly understood whether and how the GPIT complex affects primordial germ cell (PGC) development. In this study, we report the important roles of GPI transamidase in PGC migration and development in zebrafish embryos. Mutation of pigu or pigk, both encoding essential GPIT complex subunits, resulted in defective PGC migration with ectopically located PGCs and reduction of PGC counts. Notably, a detailed analysis of filopodia in PGCs revealed the attenuated polarity of filopodia distribution along the migration direction in mutant embryos. PGC transplantation and PGC-specific rescue experiments demonstrated that both PGC and somatic cell-expressed Pigu are required for PGC migration. Furthermore, expression levels of PGC-specific genes decreased in pigu mutant PGCs with the derepression of somatic cell genes. Hence, we propose that the GPIT complex plays a critical role during PGC migration and development.

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来源期刊
CiteScore
9.60
自引率
1.80%
发文量
1383
期刊介绍: The Journal of Molecular Cell Biology ( JMCB ) is a full open access, peer-reviewed online journal interested in inter-disciplinary studies at the cross-sections between molecular and cell biology as well as other disciplines of life sciences. The broad scope of JMCB reflects the merging of these life science disciplines such as stem cell research, signaling, genetics, epigenetics, genomics, development, immunology, cancer biology, molecular pathogenesis, neuroscience, and systems biology. The journal will publish primary research papers with findings of unusual significance and broad scientific interest. Review articles, letters and commentary on timely issues are also welcome. JMCB features an outstanding Editorial Board, which will serve as scientific advisors to the journal and provide strategic guidance for the development of the journal. By selecting only the best papers for publication, JMCB will provide a first rate publishing forum for scientists all over the world.
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