Lin Zexiong, Li Dongliang, Zheng Jiahuan, Yao Chencheng, Liu Dongteng, Zhang Hao, Feng Haiwei, Chen Chunxu, Li Peng, Zhang Yuxiang, Jiang Binjie, Hu Zhe, Zhao Yu, Shi Fu, Cao Dandan, Rodriguez-Wallberg Kenny A, Li Zheng, Yeung William S B, Chow Louise T, Wang Hengbin, Liu Kui
Department of Obstetrics and Gynecology, Li Ka Shing Faculty of Medicine; Shenzhen Key Laboratory of Fertility Regulation, Center of Assisted Reproduction and Embryology, The University of Hong Kong-Shenzhen Hospital, The University of Hong Kong, Hong Kong, China.
Department of Andrology, Center for Men's Health, Department of ART, Institute of Urology, Urologic Medical Center, Shanghai Key Laboratory of Reproductive Medicine, Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai 200080, China.
Cell Rep. 2024 Jan 23;43(1):113651. doi: 10.1016/j.celrep.2023.113651. Epub 2024 Jan 3.
Dynamic chromosome remodeling and nuclear compartmentalization take place during mammalian meiotic prophase I. We report here that the crucial roles of male pachynema-specific protein (MAPS) in pachynema progression might be mediated by its liquid-liquid phase separation in vitro and in cellulo. MAPS forms distinguishable liquid phases, and deletion or mutations of its N-terminal amino acids (aa) 2-9 disrupt its secondary structure and charge properties, impeding phase separation. Maps pachytene spermatocytes exhibit defects in nucleus compartmentalization, including defects in forming sex bodies, altered nucleosome composition, and disordered chromatin accessibility. Maps male mice expressing MAPS protein lacking aa 2-9 phenocopy Maps mice. Moreover, a frameshift mutation in C3orf62, the human counterpart of Maps, is correlated with nonobstructive azoospermia in a patient exhibiting pachynema arrest in spermatocyte development. Hence, the phase separation property of MAPS seems essential for pachynema progression in mouse and human spermatocytes.
动态染色体重塑和核区室化发生在哺乳动物减数分裂前期I。我们在此报告,雄性粗线期特异性蛋白(MAPS)在粗线期进程中的关键作用可能是由其在体外和细胞内的液-液相分离介导的。MAPS形成可区分的液相,其N端氨基酸(aa)2-9的缺失或突变会破坏其二级结构和电荷性质,从而阻碍相分离。Maps粗线期精母细胞在细胞核区室化方面表现出缺陷,包括性体形成缺陷、核小体组成改变和染色质可及性紊乱。表达缺少aa 2-9的MAPS蛋白的Maps雄性小鼠表现出与Maps小鼠相似的表型。此外,Maps在人类中的对应物C3orf62中的一个移码突变与一名在精母细胞发育中出现粗线期停滞的患者的非梗阻性无精子症相关。因此,MAPS的相分离特性似乎对小鼠和人类精母细胞的粗线期进程至关重要。