Terno, a cyclin-interacting protein regulating meiotic exit and sperm differentiation in Drosophila.

IF 6.1 1区 生物学 Q1 CELL BIOLOGY
Journal of Cell Biology Pub Date : 2026-10-05 Epub Date: 2026-08-13 DOI:10.1083/jcb.202511191
Elisabetta Bucciarelli, Lucia Graziadio, Claudia Pellacani, Maria Patrizia Somma, Caterina Mencarelli, Silvia Bonaccorsi, Maurizio Gatti
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引用次数: 0

Abstract

In animal systems, the only case of third meiotic division without a prior round of DNA replication has been described in Drosophila males carrying mutations in roughex, a gene encoding an inhibitor of Cdk1 activity. Here, we describe another Drosophila gene, terno (teo), that regulates meiotic exit in males. In teo mutants, meiosis I and II are regular, but in many germline cysts, the 64 haploid spermatids undergo an extra division. Additionally, teo mutants are defective in sperm individualization. Teo interacts with cyclin A and B, Fizzy (Cdc20), and the anaphase-promoting complex/cyclosome components Cdc16 and Cdc27. In teo mutant testes, the cyclin A and B levels are higher than in wild type, and downregulation of either cyclin rescues the teo mutant phenotypes. These results suggest that Teo facilitates targeted degradation of the cyclins, so that in teo mutants, there is an increase in Cdk1-CycA and Cdk1-CycB activities, resulting in both the extra meiotic division and the sperm maturation defect.

Terno,一种调节果蝇减数分裂退出和精子分化的周期蛋白相互作用蛋白。
在动物系统中,唯一没有DNA复制的第三次减数分裂发生在携带rooughex(一种编码Cdk1活性抑制剂的基因)突变的雄性果蝇中。在这里,我们描述了另一个果蝇基因,terno (teo),它调节雄性减数分裂的退出。在teo突变体中,减数分裂I和II是规则的,但在许多种系囊肿中,64个单倍体精子进行额外的分裂。此外,teo突变体在精子个体化方面存在缺陷。Teo与细胞周期蛋白A和B、Fizzy (Cdc20)以及后期促进复合物/环小体成分Cdc16和Cdc27相互作用。在teo突变型睾丸中,细胞周期蛋白A和B水平高于野生型,下调任一细胞周期蛋白均可挽救teo突变型表型。这些结果表明,Teo促进了周期蛋白的靶向降解,因此在Teo突变体中,Cdk1-CycA和Cdk1-CycB活性增加,导致减数分裂额外分裂和精子成熟缺陷。
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
Journal of Cell Biology
Journal of Cell Biology 生物-细胞生物学
CiteScore
12.60
自引率
2.60%
发文量
213
审稿时长
1 months
期刊介绍: The Journal of Cell Biology (JCB) is a comprehensive journal dedicated to publishing original discoveries across all realms of cell biology. We invite papers presenting novel cellular or molecular advancements in various domains of basic cell biology, along with applied cell biology research in diverse systems such as immunology, neurobiology, metabolism, virology, developmental biology, and plant biology. We enthusiastically welcome submissions showcasing significant findings of interest to cell biologists, irrespective of the experimental approach.
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