在果蝇精子发生过程中,Mettl3是种系功能所必需的

IF 2.2 3区 生物学 Q4 CELL BIOLOGY
Alannah Morse, Hailey Kaba, Corinne Leighty, Emily MacLean, Rosemarie Mirabella, Mary Reinaker, Rohan Harris, Jazmyn Moodie, Antonio Rockwell
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引用次数: 0

摘要

m6A修饰负责调节RNA代谢的几个方面。催化这种修饰的酶Mettl3是高度保守的,是许多生物过程(如精子发生)所必需的。在这里,我们研究了Mettl3在果蝇精子发生过程中生殖系功能中的作用。我们发现生殖系中Mettl3的缺失会导致后期精子发生的错误,这一过程被称为精子发生。在种系基因敲低中,与精子结合的肌动蛋白锥在个体化过程中不能保持紧密的包裹。肌动蛋白锥体组装的问题似乎破坏了精子发生的进程,导致废物袋缺乏,这是精子异常个体化的一个指标。这些错误导致精囊中精子很少甚至没有精子,最终导致生殖细胞敲低导致生育能力降低。此外,我们的研究结果表明Hsp60B在基因敲低中被错误调控,这可能解释了至少一些观察到的表型。总的来说,本研究的数据表明,在果蝇精子发生过程中,Mettl3在调节精细胞分化中起着重要作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Mettl3 is required for germline function during Drosophila spermatogenesis
The m6A modification is responsible for regulating several aspects of RNA metabolism. The enzyme that catalyzes this modification Mettl3, is highly conserved and required for numerous biological processes such as spermatogenesis. Here we examine the role of Mettl3 in germline function during Drosophila spermatogenesis. We find that depletion of Mettl3 in the germline results in errors in late-stage spermatogenesis, the process known as spermiogenesis. In germline knockdowns, actin cones bound to spermatids fail to remain tightly packed during the individualization process. Issues with actin cone assembly appear to disrupt progression through spermiogenesis resulting in waste bag deficiency, an indicator of abnormal spermatid individualization. These errors result in little to no sperm in seminal vesicles culminating in reduced fertility in germline knockdowns. Furthermore, our findings suggest Hsp60B is misregulated in knockdowns, which potentially explains at least some observed phenotypes. Collectively, the data presented in this investigation suggests Mettl3 has a prominent role in regulating spermatid differentiation during Drosophila spermatogenesis.
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来源期刊
Differentiation
Differentiation 生物-发育生物学
CiteScore
4.10
自引率
3.40%
发文量
38
审稿时长
51 days
期刊介绍: Differentiation is a multidisciplinary journal dealing with topics relating to cell differentiation, development, cellular structure and function, and cancer. Differentiation of eukaryotes at the molecular level and the use of transgenic and targeted mutagenesis approaches to problems of differentiation are of particular interest to the journal. The journal will publish full-length articles containing original work in any of these areas. We will also publish reviews and commentaries on topics of current interest. The principal subject areas the journal covers are: • embryonic patterning and organogenesis • human development and congenital malformation • mechanisms of cell lineage commitment • tissue homeostasis and oncogenic transformation • establishment of cellular polarity • stem cell differentiation • cell reprogramming mechanisms • stability of the differentiated state • cell and tissue interactions in vivo and in vitro • signal transduction pathways in development and differentiation • carcinogenesis and cancer • mechanisms involved in cell growth and division especially relating to cancer • differentiation in regeneration and ageing • therapeutic applications of differentiation processes.
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