研究报告

着丝粒蛋白Fta2磷酸化对减数分裂的影响

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  • 1.江南大学未来食品科学中心,无锡 214122
    2.江南大学生物工程学院,无锡 214122
倪子涵,硕士研究生,专业方向:染色体分离机制。E-mail: 641752174@qq.com

收稿日期: 2024-03-14

  修回日期: 2024-05-06

  网络出版日期: 2024-05-22

The effect of centromere protein Fta2 phosphorylation during meiosis

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  • 1. Science Center for Future Foods, Jiangnan University, Wuxi 214122, China
    2. Biotechnology School, Jiangnan University,Wuxi 214122,China

Received date: 2024-03-14

  Revised date: 2024-05-06

  Online published: 2024-05-22

摘要

在减数分裂过程中,黏连蛋白(cohesin)在着丝粒区域定位出现缺陷时会导致一系列疾病的产生。黏连蛋白的正确定位离不开装载复合体Mis4-Ssl3的参与,现已知黏连蛋白在装载复合体的帮助下完成装载过程,但是其如何在着丝粒区域定位仍不清楚。基于已有研究报道黏连蛋白在着丝粒的定位由着丝粒蛋白的磷酸化介导,本研究从Sim4着丝粒蛋白复合体组分Fta2蛋白着手,通过生物信息学手段寻找潜在的磷酸化位点,在裂殖酵母(Schizosaccharomyces pombe)中构建了fta2-9Afta2-9D突变体,并通过噻苯咪唑(thiabendazole,TBZ)敏感度测试和荧光显微定位对其表型进行检测。结果显示,Fta2蛋白的磷酸化对有丝分裂没有影响,但对减数分裂染色体分离存在影响。本研究表明Fta2的磷酸化对减数分裂非常重要,很可能与减数分裂特有的黏连蛋白定位有关。

本文引用格式

倪子涵, 闵羽, 马玲玲, 渡边嘉典 . 着丝粒蛋白Fta2磷酸化对减数分裂的影响[J]. 遗传, 2024 , 46(7) : 552 -559 . DOI: 10.16288/j.yczz.24-038

Abstract

During meiosis, defects in cohesin localization within the centromere region can result in various diseases. Accurate cohesin localization depends on the Mis4-Ssl3 loading complex. Although it is known that cohesin completes the loading process with the help of the loading complex, the mechanisms underlying its localization in the centromere region remain unclear. Previous studies suggest cohesin localization in the centromere is mediated by phosphorylation of centromeric proteins. In this study, we focused on the Fta2 protein, a component of the Sim4 centromere protein complex. Using bioinformatics methods, potential phosphorylation sites were identified, and fta2-9A and fta2-9D mutants were constructed in Schizosaccharomyces pombe. The phenotypes of these mutants were characterized through testing thiabendazole (TBZ) sensitivity and fluorescent microscopy localization. Results indicated that Fta2 phosphorylation did not impact mitosis but affected chromosome segregation during meiosis. This study suggests that Fta2 phosphorylation is vital for meiosis and may be related to the specific localization of cohesin during this process.

参考文献

[1] Tong MH. Meiosis: no end in sight. Asian J Androl, 2021, 23(6): 547-548.
[2] Ishiguro KI. The cohesin complex in mammalian meiosis. Genes Cells, 2018, 24(1): 6-30.
[3] Sakuno T, Tashiro S, Tanizawa H, Iwasaki O, Ding DQ, Haraguchi T, Noma KI, Hiraoka Y. Rec8 cohesin-mediated Axis-loop chromatin architecture is required for meiotic recombination. Nucleic Acids Res, 2022, 50(7): 3799-3816.
[4] Watanabe Y, Nurse P. Cohesin Rec8 is required for reductional chromosome segregation at meiosis. Nature, 1999, 400(6743): 461.
[5] Bernard P, Schmidt CK, Vaur S, Dheur S, Drogat J, Genier S, Ekwall K, Uhlmann F, Javerzat JP. Cell-cycle regulation of cohesin stability along fission yeast chromosomes. EMBO J, 2007, 27(1): 111-121.
[6] Zhang Yu, Fang YD. Progresses on the structure and function of cohesin. Hereditas(Beijing), 2020, 42(1): 57-72.
  张雨, 方玉达. Cohesin结构及功能研究进展. 遗传, 2020, 42(1): 57-72.
[7] Murayama Y, Uhlmann F. DNA entry into and exit out of the cohesin ring by an interlocking gate mechanism. Cell, 2015, 163(7): 1628-1640.
[8] Shi ZH, Li ZQ, Zhang GF. The mechanism of histone lysine methylation of plant involved in gene expression and regulation. Hereditas(Beijing), 2014, 36(3): 208-219.
  施子晗, 李泽琴, 张根发. 植物组蛋白赖氨酸化修饰参与基因表达调控的机理. 遗传, 2014, 36(3): 208-219.
[9] Goto YH, Yamagishi Y, Shintomi-Kawamura M, Abe M, Tanno Y, Watanabe Y. Pds5 regulates sister-chromatid cohesion and chromosome bi-orientation through a conserved protein interaction module. Curr Biol, 2017, 27(7): 1005-1012.
[10] Hinshaw SM, Makrantoni V, Harrison SC, Marston AL. The kinetochore receptor for the cohesin loading complex. Cell, 2017, 171(1): 72-84.e13.
[11] Pidoux AL, Allshire RC. Kinetochore and heterochromatin domains of the fission yeast centromere. Chromosome Res, 2004, 12(6): 521-534.
[12] Liu XK, Mcleod I, Anderson S, Yates JR, He XW. Molecular analysis of kinetochore architecture in fission yeast. EMBO J, 2005, 24(16): 2919-2930.
[13] Kerres A, Jakopec V, Beuter C, Karig I, P?hlmann J, Pidoux A, Allshire R, Fleig U. Fta2, an essential fission yeast kinetochore component, interacts closely with the conserved Mal2 protein. Mol Biol Cell, 2006, 17(10): 4167-4178.
[14] Guo XJ. The properties analysis of human centrin 1[Dissertation]. Shanxi University, 2017.
  郭小娟. 人中心蛋白1的性质研究[学位论文]. 山西大学, 2017.
[15] Zhang ZH, Kang XJ, Mu SM. Histone phosphorylation and spermatogenesis. Hereditas(Beijing), 2014, 36(3): 220-227.
  张朝晖, 康现江, 穆淑梅. 组蛋白磷酸化修饰与精子发生. 遗传, 2014, 36(3): 220-227.
[16] Minagawa M, Shirato M, Toya M, Sato M. Dual impact of a Benzimidazole resistant β-tubulin on microtubule behavior in fission yeast. Cells, 2021, 10(5): 1042.
[17] Shimoda C, Hirata A, Kishida M, Hashida T, Tanaka K. Characterization of meiosis-deficient mutants by electron microscopy and mapping of four essential genes in the fission yeast Schizosaccharomyces pombe. Mol Gen Genet, 1985, 200(2): 252-257.
[18] Kagami A, Sakuno T, Yamagishi Y, Ishiguro T, Tsukahara T, Shirahige K, Tanaka K, Watanabe Y. Acetylation regulates monopolar attachment at multiple levels during meiosis I in fission yeast. EMBO Rep, 2011, 12(11): 1189-1195.
[19] Kitajima TS, Kawashima SA, Watanabe Y. The conserved kinetochore protein shugoshin protects centromeric cohesion during meiosis. Nature, 2004, 427(6974): 510.
[20] Yokobayashi S, Watanabe Y. The kinetochore protein Moa1 enables cohesion-mediated monopolar attachment at meiosis I. Cell, 2005, 123(5): 803-817.
[21] Miyazaki S, Kim J, Yamagishi Y, Ishiguro T, Okada Y, Tanno Y, Sakuno T, Watanabe Y. Meikin-associated polo-like kinase specifies Bub1 distribution in meiosis I. Genes Cells, 2017, 22(6): 552-567.
[22] Ma W, Zhou JW, Chen J, Carr AM, Watanabe Y. Meikin synergizes with shugoshin to protect cohesin Rec8 during meiosis I. Genes Dev, 2021, 35(9-10): 692-697.
[23] Sharif WD, Glick GG, Davidson MK, Wahls WP. Distinct functions of S. pombe Rec12 (Spo11) protein and Rec12-dependent crossover recombination (chiasmata) in meiosis I; and a requirement for Rec12 in meiosis II. Cell Chromosome, 2002, 1(1): 1.
[24] Litwin I, Wysocki R. New insights into cohesin loading. Curr Genet, 2018, 64(1): 53-61.
[25] Takahashi TS, Basu A, Bermudez V, Hurwitz J, Walter JC. Cdc7-Drf1 kinase links chromosome cohesion to the initiation of DNA replication in Xenopus egg extracts. Genes Dev, 2008, 22(14): 1894-1905.
[26] Kuenzel NA, Alcázar-Román AR, Saiardi A, Bartsch SM, Daunaraviciute S, Fiedler D, Fleig U. Inositol pyrophosphate-controlled kinetochore architecture and mitotic entry in S. pombe. J Fungi (Basel), 2022, 8(9): 933.
[27] Mcainsh AD, Meraldi P. The CCAN complex: linking centromere specification to control of kinetochore- microtubule dynamics. Semin Cell Dev Biol, 2011, 22(9): 946-952.
[28] Hiraga SI, Alvino GM, Chang FJ, Lian HY, Sridhar A, Kubota T, Brewer BJ, Weinreich M, Raghuraman MK, Donaldson AD. Rif1 controls DNA replication by directing Protein Phosphatase 1 to reverse Cdc7-mediated phosphorylation of the MCM complex. Genes Dev, 2014, 28(4): 372-83.
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