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    SGO2 shugoshin 2 [ Homo sapiens (human) ]

    Gene ID: 151246, updated on 10-Oct-2024

    GeneRIFs: Gene References Into Functions

    GeneRIFPubMed TitleDate
    SGOL2 promotes prostate cancer progression by inhibiting RAB1A ubiquitination.

    SGOL2 promotes prostate cancer progression by inhibiting RAB1A ubiquitination.
    Lv T, He D, Zhang X, Guo X, Li Z, Zhang A, Fan B, Wang Z., Free PMC Article

    01/14/2023
    High SGO2 Expression Predicts Poor Overall Survival: A Potential Therapeutic Target for Hepatocellular Carcinoma.

    High SGO2 Expression Predicts Poor Overall Survival: A Potential Therapeutic Target for Hepatocellular Carcinoma.
    Deng M, Li S, Mei J, Lin W, Zou J, Wei W, Guo R., Free PMC Article

    12/11/2021
    Shugosin 2 is a biomarker for pathological grading and survival prediction in patients with gliomas.

    Shugosin 2 is a biomarker for pathological grading and survival prediction in patients with gliomas.
    Kao Y, Tsai WC, Chen SH, Hsu SY, Huang LC, Chang CJ, Huang SM, Hueng DY., Free PMC Article

    11/13/2021
    results identify an unexpected function of SGO2 in mitotically dividing cells and a mechanism of separase regulation that is independent of securin but still supervised by the spindle assembly checkpoint

    Securin-independent regulation of separase by checkpoint-induced shugoshin-MAD2.
    Hellmuth S, Gómez-H L, Pendás AM, Stemmann O.

    06/6/2020
    The SET localizes at the inner centromere by interacting directly with SGO2, with SET levels declining at increased distances between kinetochore pairs, leading to establishment of chromosome bi-orientation.

    Aurora B kinase activity is regulated by SET/TAF1 on Sgo2 at the inner centromere.
    Asai Y, Fukuchi K, Tanno Y, Koitabashi-Kiyozuka S, Kiyozuka T, Noda Y, Matsumura R, Koizumi T, Watanabe A, Nagata K, Watanabe Y, Terada Y., Free PMC Article

    05/16/2020
    Results from a study on gene expression variability markers in early-stage human embryos shows that SGO2 is a putative expression variability marker for the 3-day, 8-cell embryo stage.

    Variability of Gene Expression Identifies Transcriptional Regulators of Early Human Embryonic Development.
    Hasegawa Y, Taylor D, Ovchinnikov DA, Wolvetang EJ, de Torrenté L, Mar JC., Free PMC Article

    07/23/2018
    Molecular chaperone SET-assisted eviction of linker histones and Shugoshins is a fundamental step in mammalian mitotic progression.

    Phospho-H1 Decorates the Inter-chromatid Axis and Is Evicted along with Shugoshin by SET during Mitosis.
    Krishnan S, Smits AH, Vermeulen M, Reinberg D., Free PMC Article

    09/30/2017
    In mouse, Sgol2a encoding shugoshin-like 2a is necessary during meiosis in both sexes to maintain the integrity of the cohesin complex that tethers sister chromatids. Human SGO2 has not previously been implicated in any disorder, but in this case of POI and perhaps others, it is a candidate for unexplained infertility

    Mutations of SGO2 and CLDN14 collectively cause coincidental Perrault syndrome.
    Faridi R, Rehman AU, Morell RJ, Friedman PL, Demain L, Zahra S, Khan AA, Tohlob D, Assir MZ, Beaman G, Khan SN, Newman WG, Riazuddin S, Friedman TB., Free PMC Article

    07/1/2017
    Sgol2's ability to protect cohesin depends on its interaction with PP2A, as is its ability to silence the SAC, with the latter being mediated by direct binding to Mad2

    Sgol2 provides a regulatory platform that coordinates essential cell cycle processes during meiosis I in oocytes.
    Rattani A, Wolna M, Ploquin M, Helmhart W, Morrone S, Mayer B, Godwin J, Xu W, Stemmann O, Pendas A, Nasmyth K., Free PMC Article

    03/7/2015
    identified the phosphorylation of hSgo2 by Aurora B at the N-terminal coiled-coil region and the middle region, and showed that these phosphorylations separately promote binding of hSgo2 to PP2A and MCAK

    Phosphorylation of mammalian Sgo2 by Aurora B recruits PP2A and MCAK to centromeres.
    Tanno Y, Kitajima TS, Honda T, Ando Y, Ishiguro K, Watanabe Y., Free PMC Article

    10/23/2010
    Observational study of gene-disease association. (HuGE Navigator)

    Genetic variants in TPMT and COMT are associated with hearing loss in children receiving cisplatin chemotherapy.
    Ross CJ, Katzov-Eckert H, Dubé MP, Brooks B, Rassekh SR, Barhdadi A, Feroz-Zada Y, Visscher H, Brown AM, Rieder MJ, Rogers PC, Phillips MS, Carleton BC, Hayden MR, CPNDS Consortium.

    12/2/2009
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