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    CSPP1 centrosome and spindle pole associated protein 1 [ Homo sapiens (human) ]

    Gene ID: 79848, updated on 7-Apr-2024

    GeneRIFs: Gene References Into Functions

    GeneRIFPubMed TitleDate
    CSPP1 stabilizes growing microtubule ends and damaged lattices from the luminal side.

    CSPP1 stabilizes growing microtubule ends and damaged lattices from the luminal side.
    van den Berg CM, Volkov VA, Schnorrenberg S, Huang Z, Stecker KE, Grigoriev I, Gilani S, Frikstad KM, Patzke S, Zimmermann T, Dogterom M, Akhmanova A., Free PMC Article

    02/10/2023
    Circle RNA circCSPP1 promotes human osteosarcoma cell proliferation and increases glucose metabolism by suppressing miR-200c maturation.

    Circle RNA circCSPP1 promotes human osteosarcoma cell proliferation and increases glucose metabolism by suppressing miR-200c maturation.
    Zhang L, Yang ST, Wang C, Zhang LC, Zhang X, Li FC, Wang SY, Ma K.

    06/25/2022
    Roles of circ-CSPP1 on the proliferation and metastasis of glioma cancer.

    Roles of circ-CSPP1 on the proliferation and metastasis of glioma cancer.
    Xue YF, Li M, Li W, Lin Q, Yu BX, Zhu QB, Chen HJ.

    04/3/2021
    Tumor-promoting effect was inhibited after we transfected miR-1236-3p into circ-CSPP1 overexpressing OC cells.

    circ-CSPP1 promotes proliferation, invasion and migration of ovarian cancer cells by acting as a miR-1236-3p sponge.
    Li QH, Liu Y, Chen S, Zong ZH, Du YP, Sheng XJ, Zhao Y.

    08/31/2019
    Microtubule-independent but desmoplakin-dependent localization of CSPP-L to desmosomes occurs in apical-basal polarized epithelial cells. CSPP-L depletion promoted multi-lumen spheroid formation in Caco-2 cells.

    CSPP-L Associates with the Desmosome of Polarized Epithelial Cells and Is Required for Normal Spheroid Formation.
    Sternemalm J, Geimer S, Frikstad KA, Schink KO, Stokke T, Patzke S., Free PMC Article

    05/21/2016
    propose that CSPP1 cooperates with CENP-H on kinetochores to serve as a novel regulator of kinetochore microtubule dynamics for accurate chromosome segregation

    Mitotic Protein CSPP1 Interacts with CENP-H Protein to Coordinate Accurate Chromosome Oscillation in Mitosis.
    Zhu L, Wang Z, Wang W, Wang C, Hua S, Su Z, Brako L, Garcia-Barrio M, Ye M, Wei X, Zou H, Ding X, Liu L, Liu X, Yao X., Free PMC Article

    05/7/2016
    Differential expression of a nuclear CSPP1 isoform identified biologically and clinically distinct subgroups of basal-like breast carcinoma.

    Nuclear CSPP1 expression defined subtypes of basal-like breast cancer.
    Sternemalm J, Russnes HG, Zhao X, Risberg B, Nord S, Caldas C, Børresen-Dale AL, Stokke T, Patzke S., Free PMC Article

    11/22/2014
    CSPP1 mutations are a major cause of the Joubert-Jeune phenotype in humans.

    Mutations in CSPP1 cause primary cilia abnormalities and Joubert syndrome with or without Jeune asphyxiating thoracic dystrophy.
    Tuz K, Bachmann-Gagescu R, O'Day DR, Hua K, Isabella CR, Phelps IG, Stolarski AE, O'Roak BJ, Dempsey JC, Lourenco C, Alswaid A, Bönnemann CG, Medne L, Nampoothiri S, Stark Z, Leventer RJ, Topçu M, Cansu A, Jagadeesh S, Done S, Ishak GE, Glass IA, Shendure J, Neuhauss SC, Haldeman-Englert CR, Doherty D, Ferland RJ., Free PMC Article

    03/1/2014
    Our data suggest that CSPP1 is required for proper primary cilium formation or stability and that CSPP1 mutations result in abnormal mid-hindbrain development.

    Mutations in CSPP1 lead to classical Joubert syndrome.
    Akizu N, Silhavy JL, Rosti RO, Scott E, Fenstermaker AG, Schroth J, Zaki MS, Sanchez H, Gupta N, Kabra M, Kara M, Ben-Omran T, Rosti B, Guemez-Gamboa A, Spencer E, Pan R, Cai N, Abdellateef M, Gabriel S, Halbritter J, Hildebrandt F, van Bokhoven H, Gunel M, Gleeson JG., Free PMC Article

    03/1/2014
    mutations in CSPP1 were associated with variable ciliopathy phenotypes ranging from Joubert syndrome to the more severe Meckel-Gruber syndrome with perinatal lethality and occipital encephalocele

    Mutations in CSPP1, encoding a core centrosomal protein, cause a range of ciliopathy phenotypes in humans.
    Shaheen R, Shamseldin HE, Loucks CM, Seidahmed MZ, Ansari S, Ibrahim Khalil M, Al-Yacoub N, Davis EE, Mola NA, Szymanska K, Herridge W, Chudley AE, Chodirker BN, Schwartzentruber J, Majewski J, Katsanis N, Poizat C, Johnson CA, Parboosingh J, Boycott KM, Innes AM, Alkuraya FS., Free PMC Article

    03/1/2014
    CSPP isoforms require their common C-terminal domain to interact with Nephrocystin 8 (NPHP8/RPGRIP1L) and to form a ternary complex with NPHP8 and NPHP4.

    CSPP is a ciliary protein interacting with Nephrocystin 8 and required for cilia formation.
    Patzke S, Redick S, Warsame A, Murga-Zamalloa CA, Khanna H, Doxsey S, Stokke T., Free PMC Article

    11/27/2010
    CSPP interacts with and recruits MyoGEF to the central spindle, where MyoGEF contributes to the spatiotemporal regulation of cytokinesis.

    Centrosome/spindle pole-associated protein regulates cytokinesis via promoting the recruitment of MyoGEF to the central spindle.
    Asiedu M, Wu D, Matsumura F, Wei Q., Free PMC Article

    01/21/2010
    Taken together, CSPP and CSPP-L interact with centrosomes and microtubules and can differently affect microtubule organization.

    CSPP and CSPP-L associate with centrosomes and microtubules and differently affect microtubule organization.
    Patzke S, Stokke T, Aasheim HC.

    01/21/2010
    Novel centrosome/microtubule-associated coiled-coil protein (CSPP)is associated with centrosomes and microtubules and may play a role in the regulation of G(1)/S-phase progression and spindle assembly [CSPP].

    Identification of a novel centrosome/microtubule-associated coiled-coil protein involved in cell-cycle progression and spindle organization.
    Patzke S, Hauge H, Sioud M, Finne EF, Sivertsen EA, Delabie J, Stokke T, Aasheim HC.

    01/21/2010
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