Počet záznamů: 1  

Genetic variation in the major mitotic checkpoint genes associated with chromosomal aberrations in healthy humans

  1. 1.
    SYSNO ASEP0469310
    Druh ASEPJ - Článek v odborném periodiku
    Zařazení RIVJ - Článek v odborném periodiku
    Poddruh JČlánek ve WOS
    NázevGenetic variation in the major mitotic checkpoint genes associated with chromosomal aberrations in healthy humans
    Tvůrce(i) Försti, A. (DE)
    Frank, Ch. (DE)
    Smolková, B. (SK)
    Kazimírová, A. (SK)
    Barančoková, M. (SK)
    Vymetálková, Veronika (UEM-P) RID
    Kroupa, M. (CZ)
    Naccarati, Alessio (UEM-P)
    Vodičková, Ludmila (UEM-P) RID
    Buchancová, J. (SK)
    Dusinská, M. (SK)
    Musak, L. (SK)
    Vodička, Pavel (UEM-P) RID
    Hemminki, K. (DE)
    Zdroj.dok.Cancer letters. - : Elsevier - ISSN 0304-3835
    Roč. 380, č. 2 (2016), s. 442-446
    Poč.str.5 s.
    Jazyk dok.eng - angličtina
    Země vyd.NL - Nizozemsko
    Klíč. slovachromosomal integrity ; cytogenetics ; spindle checkpoint
    Vědní obor RIVEB - Genetika a molekulární biologie
    CEPGA15-14789S GA ČR - Grantová agentura ČR
    Institucionální podporaUEM-P - RVO:68378041
    UT WOS000383300300009
    EID SCOPUS84978639705
    DOI10.1016/j.canlet.2016.07.011
    AnotaceNon-specific chromosomal aberrations (CAs) are microscopically detected in about 1% of lymphocytes drawn from healthy persons. Causes of CAs in general population are not known but they may be related to risk of cancer. In view of the importance of the mitotic checkpoint machinery on maintaining chromosomal integrity we selected 9 variants in main checkpoint related genes (BUB1B, BUB3, MAD2L1, CENPF, ESPLI/separase, NEC, PTTGlisecurin, ZWILCH and ZWINT) for a genotyping study on samples from healthy individuals (N = 330 to 729) whose lymphocytes had an increased number of CAs compared to persons with a low number of CAs. Genetic variation in individual genes played a minor importance, consistent with the high conservation and selection pressure of the checkpoint system. However, gene pairs were significantly associated with CAs: PTTG1-ZWILCH and PTTG1-ZWINT. MAD2L1 and PTTG1 were the most common partners in any of the two-way interactions. The results suggest that interactions at the level of cohesin (PITG1) and kinetochore function (ZWINT, ZWILCH and MAD2L1) contribute to the frequency of CAs, suggesting that gene variants at different checkpoint functions appeared to be required for the formation of CAs. (C) 2016 Elsevier Ireland Ltd. All rights reserved.
    PracovištěÚstav experimentální medicíny
    KontaktLenka Koželská, lenka.kozelska@iem.cas.cz, Tel.: 241 062 218, 296 442 218
    Rok sběru2017
Počet záznamů: 1  

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