دورية أكاديمية

Rare variants in BNC2 are implicated in autosomal-dominant congenital lower urinary-tract obstruction

التفاصيل البيبلوغرافية
العنوان: Rare variants in BNC2 are implicated in autosomal-dominant congenital lower urinary-tract obstruction
المؤلفون: Kolvenbach, Caroline, Dworschak, Gabriel Clemens, Frese, Sandra, Japp, Anna Sophia, Schuster, Peggy, Wenzlitschke, Nina, Yilmaz, Öznur, Lopes, Filipa M., Pryalukhin, Alexey, Schierbaum, Luca, Zanden, Loes F. M. van der, Kause, Franziska, Schneider, Ronen, Taranta-Janusz, Katarzyna, Szczepańska, Maria, Pawlaczyk, Krzysztof, Newman, William G., Beaman, Glenda M., Stuart, Helen, Cervellione, Raimondo M., Feitz, Wouter F. J., Rooij, Iris Antonia Leonarda Martina van, Schreuder, Michiel F., Steffens, Martijn, Weber, Stefanie, Merz, Waltraut Maria, Feldkötter, Markus, Hoppe, Bernd, Thiele, Holger, Altmüller, Janine, Berg, Christoph, Kristiansen, Glen, Ludwig, Michael, Reutter, Heiko, Woolf, Adrian S., Hildebrandt, Friedhelm, Grote, Phillip, Zaniew, Marcin, Odermatt, Benjamin, Hilger, Alina Christine
سنة النشر: 2019
المجموعة: Publication Server of Goethe University Frankfurt am Main
مصطلحات موضوعية: ddc:610
الوصف: Congenital lower urinary-tract obstruction (LUTO) is caused by anatomical blockage of the bladder outflow tract or by functional impairment of urinary voiding. About three out of 10,000 pregnancies are affected. Although several monogenic causes of functional obstruction have been defined, it is unknown whether congenital LUTO caused by anatomical blockage has a monogenic cause. Exome sequencing in a family with four affected individuals with anatomical blockage of the urethra identified a rare nonsense variant (c.2557C>T [p.Arg853∗]) in BNC2, encoding basonuclin 2, tracking with LUTO over three generations. Re-sequencing BNC2 in 697 individuals with LUTO revealed three further independent missense variants in three unrelated families. In human and mouse embryogenesis, basonuclin 2 was detected in lower urinary-tract rudiments. In zebrafish embryos, bnc2 was expressed in the pronephric duct and cloaca, analogs of the mammalian lower urinary tract. Experimental knockdown of Bnc2 in zebrafish caused pronephric-outlet obstruction and cloacal dilatation, phenocopying human congenital LUTO. Collectively, these results support the conclusion that variants in BNC2 are strongly implicated in LUTO etiology as a result of anatomical blockage.
نوع الوثيقة: article in journal/newspaper
وصف الملف: application/octet-stream
اللغة: English
العلاقة: http://publikationen.ub.uni-frankfurt.de/frontdoor/index/index/docId/50264Test; urn:nbn:de:hebis:30:3-502648; https://nbn-resolving.org/urn:nbn:de:hebis:30:3-502648Test; https://doi.org/10.1016/j.ajhg.2019.03.023Test; http://publikationen.ub.uni-frankfurt.de/files/50264/container.zipTest
DOI: 10.1016/j.ajhg.2019.03.023
الإتاحة: https://doi.org/10.1016/j.ajhg.2019.03.023Test
http://publikationen.ub.uni-frankfurt.de/frontdoor/index/index/docId/50264Test
https://nbn-resolving.org/urn:nbn:de:hebis:30:3-502648Test
http://publikationen.ub.uni-frankfurt.de/files/50264/container.zipTest
حقوق: http://creativecommons.org/licenses/by-nc-nd/4.0/de/deed.deTest ; info:eu-repo/semantics/restrictedAccess
رقم الانضمام: edsbas.2D84DE08
قاعدة البيانات: BASE