Počet záznamů: 1  

Systems genetics in the rat HXB/BXH family identifies Tti2 as a pleiotropic quantitative trait gene for adult hippocampal neurogenesis and serum glucose

  1. 1.
    SYSNO ASEP0557065
    Druh ASEPJ - Článek v odborném periodiku
    Zařazení RIVJ - Článek v odborném periodiku
    Poddruh JČlánek ve WOS
    NázevSystems genetics in the rat HXB/BXH family identifies Tti2 as a pleiotropic quantitative trait gene for adult hippocampal neurogenesis and serum glucose
    Tvůrce(i) Senko, A. N. (DE)
    Overall, R. W. (DE)
    Šilhavý, Jan (FGU-C) RID, ORCID
    Mlejnek, Petr (FGU-C) RID, ORCID
    Malínská, H. (CZ)
    Hüttl, M. (CZ)
    Marková, I. (CZ)
    Fabel, K. S. (DE)
    Lu, L. (US)
    Stuchlík, Aleš (FGU-C) RID, ORCID
    Williams, R. W. (US)
    Pravenec, Michal (FGU-C) RID, ORCID
    Kempermann, G. (DE)
    Celkový počet autorů13
    Číslo článkue1009638
    Zdroj.dok.PLoS Genetics. - : Public Library of Science - ISSN 1553-7404
    Roč. 18, č. 4 (2022)
    Poč.str.35 s.
    Jazyk dok.eng - angličtina
    Země vyd.US - Spojené státy americké
    Klíč. slovaspontaneously hypertensive-rats ; triple t complex ; ataxia-telangiectasia ; sphingosine 1-phosphate ; mammalian target ; candidate genes ; nervous-system ; cell-survival ; igf-i ; expression
    Obor OECDGenetics and heredity (medical genetics to be 3)
    CEPGA20-00939S GA ČR - Grantová agentura ČR
    Způsob publikováníOpen access
    Institucionální podporaFGU-C - RVO:67985823
    UT WOS000780213300003
    EID SCOPUS85128526029
    DOI10.1371/journal.pgen.1009638
    AnotaceMetabolic and neurological disorders are often comorbid, suggesting that biological pathways which orchestrate peripheral homeostasis and the integrity of the nervous system intersect. The genetic architecture behind these relationships is still poorly described, in part because molecular processes in the human brain are very difficult to study. We thus used a rodent genetic reference population to investigate links between adult hippocampal neurogenesis-a cellular plasticity mechanism important for learning flexibility-and metabolism. We measured adult neurogenesis in the family of 30 HXB/BXH rat recombinant inbred strains, who are characterised by stable differences in metabolism, behaviour, and gene expression levels.Because DNA variants affecting distinct traits segregated into different members of the family, it was possible to determine which of the previously published phenotypes correlated to adult neurogenesis due to shared genomic sequence. We found that expression levels of Tti2-a part of a specialised protein chaperone complex regulating stability of PIKK kinases-were concomitantly influencing adult neurogenesis and serum glucose levels. In human populations hundreds of genomic variants regulate TTI2 expression, potentially affecting brain function and glucose homeostasis.
    PracovištěFyziologický ústav
    KontaktLucie Trajhanová, lucie.trajhanova@fgu.cas.cz, Tel.: 241 062 400
    Rok sběru2023
    Elektronická adresahttps://doi.org/10.1371/journal.pgen.1009638
Počet záznamů: 1  

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