Department of Gene Expression Regulation in Development, Institute of Gene Biology, Russian Academy of Sciences, Moscow 119334, Russia.
Laboratory of Cytotechnology, A.V. Zhirmunsky National Scientific Center of Marine Biology, Far Eastern Branch of the Russian Academy of Sciences, Vladivostok 690041, Russia.
Development. 2021 Sep 1;148(17). doi: 10.1242/dev.198788. Epub 2021 Sep 9.
CPEB proteins are conserved translation regulators involved in multiple biological processes. One of these proteins in Drosophila, Orb2, is a principal player in spermatogenesis. It is required for meiosis and spermatid differentiation. During the later process, orb2 mRNA and protein are localized within the developing spermatid. To evaluate the role of the orb2 mRNA 3'UTR in spermatogenesis, we used the CRISPR/Cas9 system to generate a deletion of the orb2 3'UTR, orb2R. This deletion disrupts the process of spermatid differentiation but has no apparent effect on meiosis. Differentiation abnormalities include defects in the initial polarization of the 64-cell spermatid cysts, mislocalization of mRNAs and proteins in the elongating spermatid tails, altered morphology of the elongating spermatid tails, and defects in the assembly of the individualization complex. These disruptions in differentiation appear to arise because orb2 mRNA and protein are not properly localized within the 64-cell spermatid cyst.
CPEB 蛋白是参与多种生物学过程的保守翻译调节剂。果蝇中的一种 CPEB 蛋白 Orb2 是精子发生的主要参与者。它对于减数分裂和精母细胞分化是必需的。在后期过程中,orb2mRNA 和蛋白定位于正在发育的精母细胞内。为了评估 orb2mRNA3'UTR 在精子发生中的作用,我们使用 CRISPR/Cas9 系统产生了 orb23'UTR 的缺失,orb2R。这种缺失破坏了精母细胞分化过程,但对减数分裂没有明显影响。分化异常包括 64 细胞精母细胞囊的初始极化缺陷、延长的精母细胞尾部中 mRNAs 和蛋白的定位错误、延长的精母细胞尾部形态改变以及个体发生复合物的组装缺陷。这些分化中断似乎是由于 orb2mRNA 和蛋白不能在 64 细胞精母细胞囊中正确定位引起的。