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    SPEN spen family transcriptional repressor [ Homo sapiens (human) ]

    Gene ID: 23013, updated on 17-Jun-2024

    GeneRIFs: Gene References Into Functions

    GeneRIFPubMed TitleDate
    Dissection of protein and RNA regions required for SPEN binding to XIST A-repeat RNA.

    Dissection of protein and RNA regions required for SPEN binding to XIST A-repeat RNA.
    Button AC, Hall SD, Ashley EL, McHugh CA., Free PMC Article

    02/22/2024
    SPEN induces miR-4652-3p to target HIPK2 in nasopharyngeal carcinoma.

    SPEN induces miR-4652-3p to target HIPK2 in nasopharyngeal carcinoma.
    Li Y, Lv Y, Cheng C, Huang Y, Yang L, He J, Tao X, Hu Y, Ma Y, Su Y, Wu L, Yu G, Jiang Q, Liu S, Liu X, Liu Z., Free PMC Article

    03/27/2021
    SPEN haploinsufficiency causes a neurodevelopmental disorder overlapping proximal 1p36 deletion syndrome with an episignature of X chromosomes in females.

    SPEN haploinsufficiency causes a neurodevelopmental disorder overlapping proximal 1p36 deletion syndrome with an episignature of X chromosomes in females.
    Radio FC, Pang K, Ciolfi A, Levy MA, Hernández-García A, Pedace L, Pantaleoni F, Liu Z, de Boer E, Jackson A, Bruselles A, McConkey H, Stellacci E, Lo Cicero S, Motta M, Carrozzo R, Dentici ML, McWalter K, Desai M, Monaghan KG, Telegrafi A, Philippe C, Vitobello A, Au M, Grand K, Sanchez-Lara PA, Baez J, Lindstrom K, Kulch P, Sebastian J, Madan-Khetarpal S, Roadhouse C, MacKenzie JJ, Monteleone B, Saunders CJ, Jean Cuevas JK, Cross L, Zhou D, Hartley T, Sawyer SL, Monteiro FP, Secches TV, Kok F, Schultz-Rogers LE, Macke EL, Morava E, Klee EW, Kemppainen J, Iascone M, Selicorni A, Tenconi R, Amor DJ, Pais L, Gallacher L, Turnpenny PD, Stals K, Ellard S, Cabet S, Lesca G, Pascal J, Steindl K, Ravid S, Weiss K, Castle AMR, Carter MT, Kalsner L, de Vries BBA, van Bon BW, Wevers MR, Pfundt R, Stegmann APA, Kerr B, Kingston HM, Chandler KE, Sheehan W, Elias AF, Shinde DN, Towne MC, Robin NH, Goodloe D, Vanderver A, Sherbini O, Bluske K, Hagelstrom RT, Zanus C, Faletra F, Musante L, Kurtz-Nelson EC, Earl RK, Anderlid BM, Morin G, van Slegtenhorst M, Diderich KEM, Brooks AS, Gribnau J, Boers RG, Finestra TR, Carter LB, Rauch A, Gasparini P, Boycott KM, Barakat TS, Graham JM Jr, Faivre L, Banka S, Wang T, Eichler EE, Priolo M, Dallapiccola B, Vissers LELM, Sadikovic B, Scott DA, Holder JL Jr, Tartaglia M., Free PMC Article

    03/27/2021
    our data demonstrate a role for SPEN in the regulation of primary cilia formation and cell migration in breast cancer cells, which may collectively explain why its expression is associated with time to metastasis in cohorts of patients with ERalpha-negative breast cancers.

    SPEN, a new player in primary cilia formation and cell migration in breast cancer.
    Légaré S, Chabot C, Basik M., Free PMC Article

    05/12/2018
    SPEN is a novel tumor-suppressor gene that may be clinically useful as a predictive biomarker of tamoxifen response in ERalpha-positive breast cancers.

    The Estrogen Receptor Cofactor SPEN Functions as a Tumor Suppressor and Candidate Biomarker of Drug Responsiveness in Hormone-Dependent Breast Cancers.
    Légaré S, Cavallone L, Mamo A, Chabot C, Sirois I, Magliocco A, Klimowicz A, Tonin PN, Buchanan M, Keilty D, Hassan S, Laperrière D, Mader S, Aleynikova O, Basik M.

    02/13/2016
    SPEN mutations were associated with diffuse large B-cell lymphoma with hepatitis C virus infection.

    The NOTCH pathway is recurrently mutated in diffuse large B-cell lymphoma associated with hepatitis C virus infection.
    Arcaini L, Rossi D, Lucioni M, Nicola M, Bruscaggin A, Fiaccadori V, Riboni R, Ramponi A, Ferretti VV, Cresta S, Casaluci GM, Bonfichi M, Gotti M, Merli M, Maffi A, Arra M, Varettoni M, Rattotti S, Morello L, Guerrera ML, Sciarra R, Gaidano G, Cazzola M, Paulli M., Free PMC Article

    10/17/2015
    Phosphorylation of the CK2 site on SMRT significantly increased affinity for SHARP.

    Structural insights into the recruitment of SMRT by the corepressor SHARP under phosphorylative regulation.
    Mikami S, Kanaba T, Takizawa N, Kobayashi A, Maesaki R, Fujiwara T, Ito Y, Mishima M.

    08/30/2014
    A structural study of the RNA binding properties of the RNA recognition motifs of SHARP.

    The crystal structure of the Split End protein SHARP adds a new layer of complexity to proteins containing RNA recognition motifs.
    Arieti F, Gabus C, Tambalo M, Huet T, Round A, Thore S., Free PMC Article

    08/9/2014
    These results demonstrate a role for the inactivation of SHARP transcription in DM1 biology.

    RNA steady-state defects in myotonic dystrophy are linked to nuclear exclusion of SHARP.
    Dansithong W, Jog SP, Paul S, Mohammadzadeh R, Tring S, Kwok Y, Fry RC, Marjoram P, Comai L, Reddy S., Free PMC Article

    10/15/2011
    MINT3 and MINT17 were informative for patient grouping to predict local recurrence in rectal cancer patients

    Identification of a quantitative MINT locus methylation profile predicting local regional recurrence of rectal cancer.
    de Maat MF, van de Velde CJ, Benard A, Putter H, Morreau H, van Krieken JH, Meershoek Klein-Kranenbarg E, de Graaf EJ, Tollenaar RA, Hoon DS.

    08/23/2010
    In functional assays, corepressor ETO, but not AML1/ETO, augments SHARP-mediated repression in an histone deacetylase-dependent manner.

    ETO, but not leukemogenic fusion protein AML1/ETO, augments RBP-Jkappa/SHARP-mediated repression of notch target genes.
    Salat D, Liefke R, Wiedenmann J, Borggrefe T, Oswald F., Free PMC Article

    01/21/2010
    both the androgen receptor interacting domains of the coactivator SRC1 and of the corepressor SMRT compete for interaction with the androgen receptor N-terminus

    Agonist-antagonist induced coactivator and corepressor interplay on the human androgen receptor.
    Dotzlaw H, Papaioannou M, Moehren U, Claessens F, Baniahmad A.

    01/21/2010
    Msx2-interacting protein(MINT), human interacts with the UbcH8.

    The Spen homolog Msx2-interacting nuclear target protein interacts with the E2 ubiquitin-conjugating enzyme UbcH8.
    Li J, Wang J, Yang X, Li J, Qin H, Dong X, Zhu Y, Liang L, Liang Y, Han H.

    01/21/2010
    SHARP is a novel component of the HDAC corepressor complex, recruited by RBP-Jkappa to repress transcription of target genes in the absence of activated Notch.

    SHARP is a novel component of the Notch/RBP-Jkappa signalling pathway.
    Oswald F, Kostezka U, Astrahantseff K, Bourteele S, Dillinger K, Zechner U, Ludwig L, Wilda M, Hameister H, Knöchel W, Liptay S, Schmid RM., Free PMC Article

    01/21/2010
    Pak1-SHARP interaction plays an essential role in enhancing the corepressor functions of SHARP, thereby modulating Notch signaling in human cancer cells.

    An essential role of Pak1 phosphorylation of SHARP in Notch signaling.
    Vadlamudi RK, Manavathi B, Singh RR, Nguyen D, Li F, Kumar R.

    01/21/2010
    SHARP gene and protein expression is elevated in human colon and ovarian endometrioid adenocarcinomas carrying gene defects leading to beta-catenin dysregulation.

    Drosophila split ends homologue SHARP functions as a positive regulator of Wnt/beta-catenin/T-cell factor signaling in neoplastic transformation.
    Feng Y, Bommer GT, Zhai Y, Akyol A, Hinoi T, Winer I, Lin HV, Cadigan KM, Cho KR, Fearon ER.

    01/21/2010
    the conserved function of the SPOC domain of SHARP is to mediate interaction with SMRT/NCoR corepressors, and that Spen proteins play an essential role in the repression complex

    A conserved structural motif reveals the essential transcriptional repression function of Spen proteins and their role in developmental signaling.
    Ariyoshi M, Schwabe JW., Free PMC Article

    01/21/2010
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