RNF20 Regulates Oocyte Meiotic Spindle Assembly by Recruiting TPM3 to Centromeres and Spindle Poles

Previously a ring finger protein 20 (RNF20) is found to be essential for meiotic recombination and mediates H2B ubiquitination during spermatogenesis. However, its role in meiotic division is still unknown. Here, it is shown that RNF20 is localized at both centromeres and spindle poles, and it is re...

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Published inAdvanced science Vol. 11; no. 13; pp. e2306986 - n/a
Main Authors Wang, Liying, Liu, Chao, Li, Li, Wei, Huafang, Wei, Wei, Zhou, Qiuxing, Chen, Yinghong, Meng, Tie‐Gang, Jiao, Renjie, Wang, Zhen‐Bo, Sun, Qing‐Yuan, Li, Wei
Format Journal Article
LanguageEnglish
Published Germany John Wiley & Sons, Inc 01.04.2024
John Wiley and Sons Inc
Wiley
Subjects
Antibodies
Centromere
Chromosomes
Experiments
Female
Females
Humans
Infertility
Localization
Male
Meiosis
oocyte maturation
Oocytes - metabolism
Ovaries
Physiology
Proteins
Puberty
RNF20
Spindle Apparatus - metabolism
spindle assembly
Spindle Poles - metabolism
Statistical analysis
Student's t-test
TPM3
RNF20
meiosis
oocyte maturation
spindle assembly
TPM3
Online AccessGet full text

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Abstract Previously a ring finger protein 20 (RNF20) is found to be essential for meiotic recombination and mediates H2B ubiquitination during spermatogenesis. However, its role in meiotic division is still unknown. Here, it is shown that RNF20 is localized at both centromeres and spindle poles, and it is required for oocyte acentrosomal spindle organization and female fertility. RNF20‐depleted oocytes exhibit severely abnormal spindle and chromosome misalignment caused by defective bipolar organization. Notably, it is found that the function of RNF20 in spindle assembly is not dependent on its E3 ligase activity. Instead, RNF20 regulates spindle assembly by recruiting tropomyosin3 (TPM3) to both centromeres and spindle poles with its coiled‐coil motif. The RNF20‐TPM3 interaction is essential for acentrosomal meiotic spindle assembly. Together, the studies uncover a novel function for RNF20 in mediating TPM3 recruitment to both centromeres and spindle poles during oocyte spindle assembly. It is shown that RNF20 is a key regulator for acentrosomal spindle assembly and first meiosis completion in oocytes. It is found that the RNF20‐TPM3 interaction is essential for acentrosomal meiotic spindle assembly. RNF20 regulates spindle assembly by recruiting TPM3 to centromeres and spindle poles, which is independent on its E3 ligase activity.
AbstractList Previously a ring finger protein 20 (RNF20) is found to be essential for meiotic recombination and mediates H2B ubiquitination during spermatogenesis. However, its role in meiotic division is still unknown. Here, it is shown that RNF20 is localized at both centromeres and spindle poles, and it is required for oocyte acentrosomal spindle organization and female fertility. RNF20‐depleted oocytes exhibit severely abnormal spindle and chromosome misalignment caused by defective bipolar organization. Notably, it is found that the function of RNF20 in spindle assembly is not dependent on its E3 ligase activity. Instead, RNF20 regulates spindle assembly by recruiting tropomyosin3 (TPM3) to both centromeres and spindle poles with its coiled‐coil motif. The RNF20‐TPM3 interaction is essential for acentrosomal meiotic spindle assembly. Together, the studies uncover a novel function for RNF20 in mediating TPM3 recruitment to both centromeres and spindle poles during oocyte spindle assembly. It is shown that RNF20 is a key regulator for acentrosomal spindle assembly and first meiosis completion in oocytes. It is found that the RNF20‐TPM3 interaction is essential for acentrosomal meiotic spindle assembly. RNF20 regulates spindle assembly by recruiting TPM3 to centromeres and spindle poles, which is independent on its E3 ligase activity.
Previously a ring finger protein 20 (RNF20) is found to be essential for meiotic recombination and mediates H2B ubiquitination during spermatogenesis. However, its role in meiotic division is still unknown. Here, it is shown that RNF20 is localized at both centromeres and spindle poles, and it is required for oocyte acentrosomal spindle organization and female fertility. RNF20‐depleted oocytes exhibit severely abnormal spindle and chromosome misalignment caused by defective bipolar organization. Notably, it is found that the function of RNF20 in spindle assembly is not dependent on its E3 ligase activity. Instead, RNF20 regulates spindle assembly by recruiting tropomyosin3 (TPM3) to both centromeres and spindle poles with its coiled‐coil motif. The RNF20‐TPM3 interaction is essential for acentrosomal meiotic spindle assembly. Together, the studies uncover a novel function for RNF20 in mediating TPM3 recruitment to both centromeres and spindle poles during oocyte spindle assembly.
Abstract Previously a ring finger protein 20 (RNF20) is found to be essential for meiotic recombination and mediates H2B ubiquitination during spermatogenesis. However, its role in meiotic division is still unknown. Here, it is shown that RNF20 is localized at both centromeres and spindle poles, and it is required for oocyte acentrosomal spindle organization and female fertility. RNF20‐depleted oocytes exhibit severely abnormal spindle and chromosome misalignment caused by defective bipolar organization. Notably, it is found that the function of RNF20 in spindle assembly is not dependent on its E3 ligase activity. Instead, RNF20 regulates spindle assembly by recruiting tropomyosin3 (TPM3) to both centromeres and spindle poles with its coiled‐coil motif. The RNF20‐TPM3 interaction is essential for acentrosomal meiotic spindle assembly. Together, the studies uncover a novel function for RNF20 in mediating TPM3 recruitment to both centromeres and spindle poles during oocyte spindle assembly.
Previously a ring finger protein 20 (RNF20) is found to be essential for meiotic recombination and mediates H2B ubiquitination during spermatogenesis. However, its role in meiotic division is still unknown. Here, it is shown that RNF20 is localized at both centromeres and spindle poles, and it is required for oocyte acentrosomal spindle organization and female fertility. RNF20-depleted oocytes exhibit severely abnormal spindle and chromosome misalignment caused by defective bipolar organization. Notably, it is found that the function of RNF20 in spindle assembly is not dependent on its E3 ligase activity. Instead, RNF20 regulates spindle assembly by recruiting tropomyosin3 (TPM3) to both centromeres and spindle poles with its coiled-coil motif. The RNF20-TPM3 interaction is essential for acentrosomal meiotic spindle assembly. Together, the studies uncover a novel function for RNF20 in mediating TPM3 recruitment to both centromeres and spindle poles during oocyte spindle assembly.Previously a ring finger protein 20 (RNF20) is found to be essential for meiotic recombination and mediates H2B ubiquitination during spermatogenesis. However, its role in meiotic division is still unknown. Here, it is shown that RNF20 is localized at both centromeres and spindle poles, and it is required for oocyte acentrosomal spindle organization and female fertility. RNF20-depleted oocytes exhibit severely abnormal spindle and chromosome misalignment caused by defective bipolar organization. Notably, it is found that the function of RNF20 in spindle assembly is not dependent on its E3 ligase activity. Instead, RNF20 regulates spindle assembly by recruiting tropomyosin3 (TPM3) to both centromeres and spindle poles with its coiled-coil motif. The RNF20-TPM3 interaction is essential for acentrosomal meiotic spindle assembly. Together, the studies uncover a novel function for RNF20 in mediating TPM3 recruitment to both centromeres and spindle poles during oocyte spindle assembly.
Author Liu, Chao
Li, Li
Zhou, Qiuxing
Meng, Tie‐Gang
Sun, Qing‐Yuan
Wang, Liying
Wei, Wei
Li, Wei
Wei, Huafang
Chen, Yinghong
Wang, Zhen‐Bo
Jiao, Renjie
AuthorAffiliation 4 Guangzhou Key Laboratory of Metabolic Diseases and Reproductive Health Guangdong‐Hong Kong Metabolism & Reproduction Joint Laboratory Reproductive Medicine Center Guangdong Second Provincial General Hospital Guangzhou 510317 China
5 The State Key Laboratory of Respiratory Disease Guangzhou Medical University Guangzhou Guangdong 510182 China
2 State Key Laboratory of Stem Cell and Reproductive Biology Institute of Zoology Stem Cell and Regenerative Medicine Innovation Institute Chinese Academy of Sciences Beijing 100101 China
1 Guangzhou Women and Children's Medical Center Guangzhou Medical University Guangzhou 510623 China
3 University of Chinese Academy of Sciences Beijing 100049 China
AuthorAffiliation_xml – name: 3 University of Chinese Academy of Sciences Beijing 100049 China
– name: 1 Guangzhou Women and Children's Medical Center Guangzhou Medical University Guangzhou 510623 China
– name: 2 State Key Laboratory of Stem Cell and Reproductive Biology Institute of Zoology Stem Cell and Regenerative Medicine Innovation Institute Chinese Academy of Sciences Beijing 100101 China
– name: 4 Guangzhou Key Laboratory of Metabolic Diseases and Reproductive Health Guangdong‐Hong Kong Metabolism & Reproduction Joint Laboratory Reproductive Medicine Center Guangdong Second Provincial General Hospital Guangzhou 510317 China
– name: 5 The State Key Laboratory of Respiratory Disease Guangzhou Medical University Guangzhou Guangdong 510182 China
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Issue 13
Keywords RNF20
meiosis
oocyte maturation
spindle assembly
TPM3
Language English
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Snippet Previously a ring finger protein 20 (RNF20) is found to be essential for meiotic recombination and mediates H2B ubiquitination during spermatogenesis. However,...
Abstract Previously a ring finger protein 20 (RNF20) is found to be essential for meiotic recombination and mediates H2B ubiquitination during spermatogenesis....
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StartPage e2306986
SubjectTerms Antibodies
Centromere
Chromosomes
Experiments
Female
Females
Humans
Infertility
Localization
Male
Meiosis
oocyte maturation
Oocytes - metabolism
Ovaries
Physiology
Proteins
Puberty
RNF20
Spindle Apparatus - metabolism
spindle assembly
Spindle Poles - metabolism
Statistical analysis
Student's t-test
TPM3
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  priority: 102
  providerName: Wiley-Blackwell
Title RNF20 Regulates Oocyte Meiotic Spindle Assembly by Recruiting TPM3 to Centromeres and Spindle Poles
URI https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fadvs.202306986
https://www.ncbi.nlm.nih.gov/pubmed/38240347
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https://pubmed.ncbi.nlm.nih.gov/PMC10987117
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