دورية أكاديمية
Rare variants in BNC2 are implicated in autosomal-dominant congenital lower urinary-tract obstruction
العنوان: | Rare variants in BNC2 are implicated in autosomal-dominant congenital lower urinary-tract obstruction |
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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 |
DOI: | 10.1016/j.ajhg.2019.03.023 |
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