Nuclear translocation of MTL5 from cytoplasm requires its direct interaction with LIN9 and is essential for male meiosis and fertility.

Meiosis is essential for the generation of gametes and sexual reproduction, yet the factors and underlying mechanisms regulating meiotic progression remain largely unknown. Here, we showed that MTL5 translocates into nuclei of spermatocytes during zygotene-pachytene transition and ensures meiosis ad...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: Xingxia Zhang, Ming Li, Xiaohua Jiang, Hui Ma, Suixing Fan, Yang Li, Changping Yu, Jianze Xu, Ranjha Khan, Hanwei Jiang, Qinghua Shi
Formato: article
Lenguaje:EN
Publicado: Public Library of Science (PLoS) 2021
Materias:
Acceso en línea:https://doaj.org/article/22465a6b721242288bb3e3dee9e687bc
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
id oai:doaj.org-article:22465a6b721242288bb3e3dee9e687bc
record_format dspace
spelling oai:doaj.org-article:22465a6b721242288bb3e3dee9e687bc2021-12-02T20:02:52ZNuclear translocation of MTL5 from cytoplasm requires its direct interaction with LIN9 and is essential for male meiosis and fertility.1553-73901553-740410.1371/journal.pgen.1009753https://doaj.org/article/22465a6b721242288bb3e3dee9e687bc2021-08-01T00:00:00Zhttps://doi.org/10.1371/journal.pgen.1009753https://doaj.org/toc/1553-7390https://doaj.org/toc/1553-7404Meiosis is essential for the generation of gametes and sexual reproduction, yet the factors and underlying mechanisms regulating meiotic progression remain largely unknown. Here, we showed that MTL5 translocates into nuclei of spermatocytes during zygotene-pachytene transition and ensures meiosis advances beyond pachytene stage. MTL5 shows strong interactions with MuvB core complex components, a well-known transcriptional complex regulating mitotic progression, and the zygotene-pachytene transition of MTL5 is mediated by its direct interaction with the component LIN9, through MTL5 C-terminal 443-475 residues. Male Mtl5c-mu/c-mu mice expressing the truncated MTL5 (p.Ser445Arg fs*3) that lacks the interaction with LIN9 and is detained in cytoplasm showed male infertility and spermatogenic arrest at pachytene stage, same as that of Mtl5 knockout mice, indicating that the interaction with LIN9 is essential for the nuclear translocation and function of MTL5 during meiosis. Our data demonstrated MTL5 translocates into nuclei during the zygotene-pachytene transition to initiate its function along with the MuvB core complex in pachytene spermatocytes, highlighting a new mechanism regulating the progression of male meiosis.Xingxia ZhangMing LiXiaohua JiangHui MaSuixing FanYang LiChangping YuJianze XuRanjha KhanHanwei JiangQinghua ShiPublic Library of Science (PLoS)articleGeneticsQH426-470ENPLoS Genetics, Vol 17, Iss 8, p e1009753 (2021)
institution DOAJ
collection DOAJ
language EN
topic Genetics
QH426-470
spellingShingle Genetics
QH426-470
Xingxia Zhang
Ming Li
Xiaohua Jiang
Hui Ma
Suixing Fan
Yang Li
Changping Yu
Jianze Xu
Ranjha Khan
Hanwei Jiang
Qinghua Shi
Nuclear translocation of MTL5 from cytoplasm requires its direct interaction with LIN9 and is essential for male meiosis and fertility.
description Meiosis is essential for the generation of gametes and sexual reproduction, yet the factors and underlying mechanisms regulating meiotic progression remain largely unknown. Here, we showed that MTL5 translocates into nuclei of spermatocytes during zygotene-pachytene transition and ensures meiosis advances beyond pachytene stage. MTL5 shows strong interactions with MuvB core complex components, a well-known transcriptional complex regulating mitotic progression, and the zygotene-pachytene transition of MTL5 is mediated by its direct interaction with the component LIN9, through MTL5 C-terminal 443-475 residues. Male Mtl5c-mu/c-mu mice expressing the truncated MTL5 (p.Ser445Arg fs*3) that lacks the interaction with LIN9 and is detained in cytoplasm showed male infertility and spermatogenic arrest at pachytene stage, same as that of Mtl5 knockout mice, indicating that the interaction with LIN9 is essential for the nuclear translocation and function of MTL5 during meiosis. Our data demonstrated MTL5 translocates into nuclei during the zygotene-pachytene transition to initiate its function along with the MuvB core complex in pachytene spermatocytes, highlighting a new mechanism regulating the progression of male meiosis.
format article
author Xingxia Zhang
Ming Li
Xiaohua Jiang
Hui Ma
Suixing Fan
Yang Li
Changping Yu
Jianze Xu
Ranjha Khan
Hanwei Jiang
Qinghua Shi
author_facet Xingxia Zhang
Ming Li
Xiaohua Jiang
Hui Ma
Suixing Fan
Yang Li
Changping Yu
Jianze Xu
Ranjha Khan
Hanwei Jiang
Qinghua Shi
author_sort Xingxia Zhang
title Nuclear translocation of MTL5 from cytoplasm requires its direct interaction with LIN9 and is essential for male meiosis and fertility.
title_short Nuclear translocation of MTL5 from cytoplasm requires its direct interaction with LIN9 and is essential for male meiosis and fertility.
title_full Nuclear translocation of MTL5 from cytoplasm requires its direct interaction with LIN9 and is essential for male meiosis and fertility.
title_fullStr Nuclear translocation of MTL5 from cytoplasm requires its direct interaction with LIN9 and is essential for male meiosis and fertility.
title_full_unstemmed Nuclear translocation of MTL5 from cytoplasm requires its direct interaction with LIN9 and is essential for male meiosis and fertility.
title_sort nuclear translocation of mtl5 from cytoplasm requires its direct interaction with lin9 and is essential for male meiosis and fertility.
publisher Public Library of Science (PLoS)
publishDate 2021
url https://doaj.org/article/22465a6b721242288bb3e3dee9e687bc
work_keys_str_mv AT xingxiazhang nucleartranslocationofmtl5fromcytoplasmrequiresitsdirectinteractionwithlin9andisessentialformalemeiosisandfertility
AT mingli nucleartranslocationofmtl5fromcytoplasmrequiresitsdirectinteractionwithlin9andisessentialformalemeiosisandfertility
AT xiaohuajiang nucleartranslocationofmtl5fromcytoplasmrequiresitsdirectinteractionwithlin9andisessentialformalemeiosisandfertility
AT huima nucleartranslocationofmtl5fromcytoplasmrequiresitsdirectinteractionwithlin9andisessentialformalemeiosisandfertility
AT suixingfan nucleartranslocationofmtl5fromcytoplasmrequiresitsdirectinteractionwithlin9andisessentialformalemeiosisandfertility
AT yangli nucleartranslocationofmtl5fromcytoplasmrequiresitsdirectinteractionwithlin9andisessentialformalemeiosisandfertility
AT changpingyu nucleartranslocationofmtl5fromcytoplasmrequiresitsdirectinteractionwithlin9andisessentialformalemeiosisandfertility
AT jianzexu nucleartranslocationofmtl5fromcytoplasmrequiresitsdirectinteractionwithlin9andisessentialformalemeiosisandfertility
AT ranjhakhan nucleartranslocationofmtl5fromcytoplasmrequiresitsdirectinteractionwithlin9andisessentialformalemeiosisandfertility
AT hanweijiang nucleartranslocationofmtl5fromcytoplasmrequiresitsdirectinteractionwithlin9andisessentialformalemeiosisandfertility
AT qinghuashi nucleartranslocationofmtl5fromcytoplasmrequiresitsdirectinteractionwithlin9andisessentialformalemeiosisandfertility
_version_ 1718375647095554048