Differential splice isoforms of mouse CDK2 play functionally redundant roles during mitotic and meiotic division

In most mammals, the cell cycle kinase cyclin-dependent kinase 2 (CDK2) is expressed as two major isoforms as a result of alternative splicing. The shorter CDK2 isoform, CDK2S, is expressed constitutively during the cell cycle and can be detected in several tissues. In contrast, the longer isoform, CDK2L, shows preferential expression in meiotically dividing cells and upon S-phase entry in the mitotic cycle. Both CDK2L and CDK2S form heteromeric complexes with cyclins A2 and E1 in vitro. However, complexes composed of each isoform differ considerably in their kinase activity towards known CDK substrates. It is currently unknown whether the long and short isoforms of CDK2 play functionally different roles in vivo during either mitotic or meiotic divisions as conventional knockout methodology deletes both of the isoforms. Therefore, we generated mice expressing only CDK2S or CDK2L and found that both CDK2L and CDK2S are sufficient to support both mitotic and meiotic division when expressed in the absence of the other. These data contribute to the explanation of the apparent tolerance of the evolutionary loss of CDK2L expression in humans.

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Publication Details

Journal
Journal of Cell Science
Published
2025-09-22
DOI
https://doi.org/10.1242/jcs.264291
Primary Topic
Microtubule and mitosis dynamics
Type
article
Field-Weighted Citation Impact
0.00

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article

Differential splice isoforms of mouse CDK2 play functionally redundant roles during mitotic and meiotic division

Jin Rong Ow, Umur Keles, Tommaso Tabaglio, Nathan Palmer et al.
Journal of Cell Science
Microtubule and mitosis dynamics
article

Differential splice isoforms of mouse CDK2 play functionally redundant roles during mitotic and meiotic division

Jin Rong Ow, Umur Keles, Tommaso Tabaglio, Nathan Palmer, Philipp Kaldis, S. Zakiah A. Talib, Li Na Zhao, Ernesto Guccione, Christine M. F. Goh, Hanna Hultén, Kui Liu, Nisan Ece Kalem-Yapar
article en

Abstract

In most mammals, the cell cycle kinase cyclin-dependent kinase 2 (CDK2) is expressed as two major isoforms as a result of alternative splicing. The shorter CDK2 isoform, CDK2S, is expressed constitutively during the cell cycle and can be detected in several tissues. In contrast, the longer isoform, CDK2L, shows preferential expression in meiotically dividing cells and upon S-phase entry in the mitotic cycle. Both CDK2L and CDK2S form heteromeric complexes with cyclins A2 and E1 in vitro. However, complexes composed of each isoform differ considerably in their kinase activity towards known CDK substrates. It is currently unknown whether the long and short isoforms of CDK2 play functionally different roles in vivo during either mitotic or meiotic divisions as conventional knockout methodology deletes both of the isoforms. Therefore, we generated mice expressing only CDK2S or CDK2L and found that both CDK2L and CDK2S are sufficient to support both mitotic and meiotic division when expressed in the absence of the other. These data contribute to the explanation of the apparent tolerance of the evolutionary loss of CDK2L expression in humans.

Journal of Cell ScienceVol. 138(19)
Agency for Science, Technology and Research (SG), Lund University (SE), Max Perutz Labs (AT), Institute of Molecular and Cell Biology (RU), Tisch Hospital (US), University of Hong Kong - Shenzhen Hospital (CN), Angiologica (Italy) (IT), Urologische Klinik München (DE), Institute of Molecular and Cell Biology (SG), Ludwig-Maximilians-Universität München (DE), University of Hong Kong (HK), Icahn School of Medicine at Mount Sinai (US)
Stiftelsen för Strategisk Forskning, Cancerfonden, Lunds Universitet, Vetenskapsrådet, Medicinska Fakulteten, Lunds Universitet
Openalex Percentile: Top 73%
Microtubule and mitosis dynamics
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