RpL38 modulates germ cell differentiation by controlling Bam expression in Drosophila testis.

IF 8 2区 生物学 Q1 BIOLOGY Science China Life Sciences Pub Date : 2024-11-01 Epub Date: 2024-08-21 DOI:10.1007/s11427-024-2646-3
Yang Fang, Fengchao Zhang, Fangzhen Zhao, Jiajia Wang, Xinkai Cheng, Fei Ye, Jiayu He, Long Zhao, Ying Su
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Abstract

Switching from mitotic spermatogonia to meiotic spermatocytes is critical to producing haploid sperms during male germ cell differentiation. However, the underlying mechanisms of this switch remain largely unexplored. In Drosophila melanogaster, the gene RpL38 encodes the ribosomal protein L38, one component of the 60S subunit of ribosomes. We found that its depletion in spermatogonia severely diminished the production of mature sperms and thus led to the infertility of male flies. By examining the germ cell differentiation in testes, we found that RpL38-knockdown blocked the transition from spermatogonia to spermatocytes and accumulated spermatogonia in the testis. To understand the intrinsic reason for this blockage, we conducted proteomic analysis for these spermatogonia populations. Differing from the control spermatogonia, the accumulated spermatogonia in RpL38-knockdown testes already expressed many spermatocyte markers but lacked many meiosis-related proteins, suggesting that spermatogonia need to prepare some important proteins for meiosis to complete their switch into spermatocytes. Mechanistically, we found that the expression of bag of marbles (bam), a crucial determinant in the transition from spermatogonia to spermatocytes, was inhibited at both the mRNA and protein levels upon RpL38 depletion. We also confirmed that the bam loss phenocopied RpL38 RNAi in the testis phenotype and transcriptomic profiling. Strikingly, overexpressing bam was able to fully rescue the testis abnormality and infertility of RpL38-knockdown flies, indicating that bam is the key effector downstream of RpL38 to regulate spermatogonia differentiation. Overall, our data suggested that germ cells start to prepare meiosis-related proteins as early as the spermatogonial stage, and RpL38 in spermatogonia is required to regulate their transition toward spermatocytes in a bam-dependent manner, providing new knowledge for our understanding of the transition process from spermatogonia to spermatocytes in Drosophila spermatogenesis.

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RpL38通过控制果蝇睾丸中Bam的表达调节生殖细胞分化
在雄性生殖细胞分化过程中,从有丝分裂精原细胞到减数分裂精母细胞的转换是产生单倍体精子的关键。然而,这种转换的内在机制在很大程度上仍未得到探索。在黑腹果蝇中,RpL38 基因编码核糖体蛋白 L38,它是核糖体 60S 亚基的一个组成部分。我们发现,精原细胞中该基因的缺失会严重减少成熟精子的产生,从而导致雄蝇不育。通过研究睾丸中生殖细胞的分化,我们发现 RpL38 的敲除阻断了精原细胞向精母细胞的转变,并在睾丸中积累了精原细胞。为了了解这种阻滞的内在原因,我们对这些精原细胞群进行了蛋白质组分析。与对照组精原细胞不同,RpL38敲除后的睾丸中积累的精原细胞已经表达了许多精母细胞标志物,但却缺乏许多减数分裂相关蛋白,这表明精原细胞需要为减数分裂准备一些重要蛋白才能完成向精母细胞的转变。从机理上讲,我们发现精原细胞向精母细胞转变过程中的一个重要决定因素--弹珠袋(bam)的表达在RpL38缺失后的mRNA和蛋白水平上都受到了抑制。我们还证实,在睾丸表型和转录组图谱分析中,bam缺失与RpL38 RNAi表型相同。令人震惊的是,过表达bam能够完全挽救RpL38敲除蝇的睾丸异常和不育,这表明bam是RpL38下游调控精原细胞分化的关键效应物。总之,我们的数据表明,生殖细胞早在精原细胞阶段就开始准备减数分裂相关蛋白,而精原细胞中的RpL38需要以依赖bam的方式调控精原细胞向精母细胞的转变,这为我们了解果蝇精子发生过程中精原细胞向精母细胞的转变过程提供了新的知识。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
15.10
自引率
8.80%
发文量
2907
审稿时长
3.2 months
期刊介绍: Science China Life Sciences is a scholarly journal co-sponsored by the Chinese Academy of Sciences and the National Natural Science Foundation of China, and it is published by Science China Press. The journal is dedicated to publishing high-quality, original research findings in both basic and applied life science research.
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