Evidence map›Paper›PMID 40633837›Full record

ArticleJournal of advanced research2026

Tankyrase activity is essential for asymmetric division and chromosome segregation in oocyte meiosis.

Ping-Shuang Lu, Zhen-Nan Pan, Wen-Lin Pan, Yuan-Jing Zou, Rui-Jie Ma, Kun-Huan Zhang, Yue Wang, Shao-Chen Sun

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Article in Journal of advanced research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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2citing papers in PubMed
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3 · Its place in the literature

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2 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Ping-Shuang LuCollege of Animal Science and Technology, Nanjing Agricultural University, Nanjing 210095, China.
Zhen-Nan PanCollege of Animal Science and Technology, Nanjing Agricultural University, Nanjing 210095, China.
Wen-Lin PanCollege of Animal Science and Technology, Nanjing Agricultural University, Nanjing 210095, China.
Yuan-Jing ZouCollege of Animal Science and Technology, Nanjing Agricultural University, Nanjing 210095, China.
Rui-Jie MaCollege of Animal Science and Technology, Nanjing Agricultural University, Nanjing 210095, China.
Kun-Huan ZhangCollege of Animal Science and Technology, Nanjing Agricultural University, Nanjing 210095, China.
Yue WangCollege of Animal Science and Technology, Nanjing Agricultural University, Nanjing 210095, China.
Shao-Chen SunCollege of Animal Science and Technology, Nanjing Agricultural University, Nanjing 210095, China; Key Laboratory of Research on Clinical Molecular Diagnosis for High Incidence Diseases in Western Guangxi of Guangxi Higher Education Institutions, Reproductive Medicine of Guangxi Medical and Health Key Discipline Construction Project, Affiliated Hospital of Youjiang Medical University for Nationalities, Baise, China. Electronic address: sunsc@njau.edu.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionTankyrase (TNKS) is a poly ADP-ribose polymerase which is known to regulate DNA repair, GLUT4-related vesicles transportation, and mitotic sister telomeres resolution.

objectivesIn the present study, we reported the novel roles of TNKS in oocyte meiosis.

methodsUsing specific chemical inhibitors, Western blot, immunofluorescence staining, mass spectrometry, co-immunoprecipitation, and siRNA interference, we disturbed TNKS activity or depleted TNKS expression to investigate the underlying mechanisms.

resultsOur results showed that TNKS associated with microtubules, and upon loss of TNKS activity, unique phenotypes were observed in oocytes where symmetric division and improper chromosome segregation occurred simultaneously during meiotic maturation. Mass spectrometry data indicated interactions between TNKS and proteins involved in actin filaments, microtubule organization, and cell cycle. Further analysis revealed that TNKS strikingly regulated actin filaments for chromosome-spindle complex motility and cortical polarity establishment through Formin2 and Ran/N-WASP/ARP2 pathways, which are crucial for meiotic asymmetric division. Additionally, we found that TNKS associated with p-PLK1 and affected K40 acetylation of α-Tubulin, and it also regulated BubR1 transportation to kinetochore and synthesis or activity of MPF/Securin, all of which contributed to the formation of meiotic bipolar spindle and precise chromosome separation associated with the cell cycle.

conclusionsTaken together, our results suggested that poly ADP-ribose polymerase TNKS was required for actin dynamics and cell cycle, which contributed to both asymmetric division and proper chromosome segregation in mouse oocytes.

Indexed as

Asymmetric Cell DivisionChromosome SegregationMeiosisOocytesTankyrasesActin CytoskeletonAnimalsCell Cycle ProteinsFemaleKinetochoresMiceMicrotubulesPolo-Like Kinase 1Protein Serine-Threonine KinasesProto-Oncogene ProteinsSpindle ApparatusBub1b protein, mouseCell Cycle ProteinsPolo-Like Kinase 1Protein Serine-Threonine KinasesProto-Oncogene ProteinsTankyrasesActin dynamicsAsymmetric divisionMeiosisOocyteTankyrase

Identifiers

PMID40633837
PMCPMC13001052

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