4.6

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2.2

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  • ISSN 1674-8301
  • CN 32-1810/R
Kaibo Lin, Shikun Zhang, Jieli Chen, Ding Yang, Mengyi Zhu, Eugene Yujun Xu. Generation and functional characterization of a conditional Pumilio2 null allele[J]. The Journal of Biomedical Research, 2018, 32(6): 434-441. DOI: 10.7555/JBR.32.20170117
Citation: Kaibo Lin, Shikun Zhang, Jieli Chen, Ding Yang, Mengyi Zhu, Eugene Yujun Xu. Generation and functional characterization of a conditional Pumilio2 null allele[J]. The Journal of Biomedical Research, 2018, 32(6): 434-441. DOI: 10.7555/JBR.32.20170117

Generation and functional characterization of a conditional Pumilio2 null allele

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We would like to thank Dr. Takeshi Kurita for discussion and assistance throughout this project. We also thank Welcome Trust Sanger Institute and Northwestern Targeting and Transgenic Core facility for assistance in the generation of mutant mice. This work was supported by National Basic Research Program of China (973 program, 2013CB945201 and 2015CB-943002)

National Science Foundation of China (81270737)

Natural Science Foundation of Jiangsu Province (BK2012838)

Provincial Innovation and Entrepreneurship Grant as well as NIH grant U01 HD045871. Funding for open access charge: Provincial Shuangchuang Program.

More Information
  • Received Date: November 06, 2017
  • Revised Date: November 27, 2017
  • The highly conserved RNA binding protein PUF (Pumilio/FBF) family is present throughout eukaryotes from yeast to mammals, with critical roles in development, fertility and the nervous system. However, the function of the mammalian PUF family members remains underexplored. Our previous study reported that a gene-trap mutation of Pum2 results in a smaller testis but does not impact fertility and viability. Although the gene-trap mutation disrupted the key functional domain of PUM protein–PUM-HD (Pumilio homology domain), but still produced a chimeric Pum2-β-geo protein containing part of PUM2, raising a question if such a chimeric protein may provide any residual function or contribute to the reproductive phenotype. Here, we report the generation of a conditional PUM2 allele, when knocked out, producing no residual PUM2 and hence a complete loss-of-function allele. We also uncovered small but significant reduction of male fertility and viability in the mutants, suggesting requirement of PUM2 for male fertility and viability
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    Periodical cited type(6)

    1. Li X, Zhu M, Zang M, et al. PUMILIO-mediated translational control of somatic cell cycle program promotes folliculogenesis and contributes to ovarian cancer progression. Cell Mol Life Sci, 2022, 79(5): 279. DOI:10.1007/s00018-022-04254-w
    2. Li X, Yang J, Chen X, et al. PUM1 represses CDKN1B translation and contributes to prostate cancer progression. J Biomed Res, 2021, 35(5): 371-382. DOI:10.7555/JBR.35.20210067
    3. Christou-Kent M, Dhellemmes M, Lambert E, et al. Diversity of RNA-Binding Proteins Modulating Post-Transcriptional Regulation of Protein Expression in the Maturing Mammalian Oocyte. Cells, 2020, 9(3): 662. DOI:10.3390/cells9030662
    4. Lin K, Qiang W, Zhu M, et al. Mammalian Pum1 and Pum2 Control Body Size via Translational Regulation of the Cell Cycle Inhibitor Cdkn1b. Cell Rep, 2019, 26(9): 2434-2450. DOI:10.1016/j.celrep.2019.01.111
    5. Lin K, Zhang S, Shi Q, et al. Essential requirement of mammalian Pumilio family in embryonic development. Mol Biol Cell, 2018, 29(24): 2922-2932. DOI:10.1091/mbc.E18-06-0369
    6. Dong H, Zhu M, Meng L, et al. Pumilio2 regulates synaptic plasticity via translational repression of synaptic receptors in mice. Oncotarget, 2018, 9(63): 32134-32148. DOI:10.18632/oncotarget.24345

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