CFTR mRNA and its truncated splice variant (TRN-CFTR) are differentially expressed during collecting duct ontogeny

被引:24
作者
Huber, S
Braun, G
Burger-Kentischer, A
Reinhart, B
Luckow, B
Horster, M
机构
[1] Univ Munich, Inst Physiol, D-80336 Munich, Germany
[2] Univ Munich, Med Poliklin, D-80336 Munich, Germany
关键词
embryonic kidney; nephrogenesis; cystic fibrosis transmembrane conductance regulator; ureteric bud;
D O I
10.1016/S0014-5793(98)00112-4
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The collecting duct epithelium originates from the embryonic ureter by branching morphogenesis. Ontogeny-dependent changes of CFTR mRNA expression were assessed by quantitative reverse transcriptase-polymerase chain reaction (RT-PCR) in primary monolayer cultures of rat ureteric buds CUB) and cortical collecting ducts, microdissected at different embryonic and postnatal developmental stages. The amount of wild-type CFTR-specific PCR product in UB declined to 20% of the initial value between embryonic gestational day E15 and postnatal day P1. After birth the CFTR product increased transiently between P1 and P7 by a factor of 10 and decreased towards day P14. PCR products specific for TRN-CFTR, a truncated splice variant, however, were low in early embryonic cells, increased markedly between day E17 and P2, and reached a plateau postnatally. Therefore, mRNA encoding TRN-CFTR does not appear to have a specific embryonic-morphogenetic function. By contrast, such function is suggested for wild-type CFTR mRNA as its abundance was high in early embryonic nephrogenesis, as well as during a postnatal period shortly before branching morphogenesis is completed. (C) 1998 Federation of European Biochemical Societies.
引用
收藏
页码:362 / 366
页数:5
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