Počet záznamů: 1  

Heterozygous Loss-of-Function SEC61A1 Mutations Cause Autosomal-Dominant Tubulo-Interstitial and Glomerulocystic Kidney Disease with Anemia

  1. 1.
    SYSNO ASEP0463462
    Druh ASEPJ - Článek v odborném periodiku
    Zařazení RIVJ - Článek v odborném periodiku
    Poddruh JČlánek ve WOS
    NázevHeterozygous Loss-of-Function SEC61A1 Mutations Cause Autosomal-Dominant Tubulo-Interstitial and Glomerulocystic Kidney Disease with Anemia
    Tvůrce(i) Bolar, N. A. (BE)
    Golzio, C. (US)
    Živná, M. (CZ)
    Hayot, G. (US)
    Van Hemelrijk, C. (BE)
    Schepers, D. (BE)
    Vandeweyer, G. (BE)
    Hoischen, A. (NL)
    Huyghe, J. R. (BE)
    Raes, A. (BE)
    Matthys, E. (BE)
    Sys, E. (BE)
    Azou, M. (BE)
    Gubler, M. C. (FR)
    Praet, M. (BE)
    Van Camp, G. (BE)
    McFadden, K. (US)
    Pediaditakis, I. (US)
    Přistoupilová, A. (CZ)
    Hodaňová, K. (CZ)
    Vyleťal, P. (CZ)
    Hartmannová, H. (CZ)
    Stránecký, V. (CZ)
    Hůlková, H. (CZ)
    Barešová, V. (CZ)
    Jedličková, I. (CZ)
    Sovová, J. (CZ)
    Hnízda, Aleš (UOCHB-X)
    Kidd, K. (US)
    Bleyer, A. J. (US)
    Spong, R. S. (US)
    Vande Walle, J. (BE)
    Mortier, G. (BE)
    Brunner, H. (NL)
    Van Laer, L. (BE)
    Kmoch, S. (CZ)
    Katsanis, N. (US)
    Loeys, B. L. (BE)
    Zdroj.dok.American Journal of Human Genetics. - : Cell Press - ISSN 0002-9297
    Roč. 99, č. 1 (2016), s. 174-187
    Poč.str.14 s.
    Jazyk dok.eng - angličtina
    Země vyd.US - Spojené státy americké
    Klíč. slovaSec61 ; tubulo-interstitial kidney disease ; rare disease
    Vědní obor RIVEB - Genetika a molekulární biologie
    CEPLO1304 GA MŠMT - Ministerstvo školství, mládeže a tělovýchovy
    Institucionální podporaUOCHB-X - RVO:61388963
    UT WOS000381616600014
    EID SCOPUS84989869039
    DOI10.1016/j.ajhg.2016.05.028
    AnotaceAutosomal-dominant tubulo-interstitial kidney disease (ADTKD) encompasses a group of disorders characterized by renal tubular and interstitial abnormalities, leading to slow progressive loss of kidney function requiring dialysis and kidney transplantation. Mutations in UMOD, MUC1, and REN are responsible for many, but not all, cases of ADTKD. We report on two families with ADTKD and congenital anemia accompanied by either intrauterine growth retardation or neutropenia. Ultrasound and kidney biopsy revealed small dysplastic kidneys with cysts and tubular atrophy with secondary glomerular sclerosis, respectively. Exclusion of known ADTKD genes coupled with linkage analysis, whole-exome sequencing, and targeted re-sequencing identified heterozygous missense variants in SEC61A1-c.553A>G (p.Thr185Ala) and c.200T > G (p.Val67Gly)-both affecting functionally important and conserved residues in SEC61. Both transiently expressed SEC6A1A variants are delocalized to the Golgi, a finding confirmed in a renal biopsy from an affected individual. Suppression or CRISPR-mediated deletions of sec61al2 in zebrafish embryos induced convolution defects of the pronephric tubules but not the pronephric ducts, consistent with the tubular atrophy observed in the affected individuals. Human mRNA encoding either of the two pathogenic alleles failed to rescue this phenotype as opposed to a complete rescue by human wild-type mRNA. Taken together, these findings provide a mechanism by which mutations in SEC61A1 lead to an autosomal-dominant syndromic form of progressive chronic kidney disease. We highlight protein translocation defects across the endoplasmic reticulum membrane, the principal role of the SEC61 complex, as a contributory pathogenic mechanism for ADTKD.
    PracovištěÚstav organické chemie a biochemie
    Kontaktasep@uochb.cas.cz ; Kateřina Šperková, Tel.: 232 002 584 ; Viktorie Chládková, Tel.: 232 002 434
    Rok sběru2017
    Elektronická adresahttp://www.sciencedirect.com/science/article/pii/S0002929716301999
Počet záznamů: 1  

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