Expression and knockdown of zebrafish folliculin suggests requirement for embryonic brain morphogenesis.

ABSTRACT:

Background

Birt-Hogg-Dubé syndrome (BHD) is a dominantly inherited familial cancer syndrome characterised by the development of benign skin fibrofolliculomas, multiple lung and kidney cysts, spontaneous pneumothorax and susceptibility to renal cell carcinoma. BHD is caused by mutations in the gene encoding Folliculin (FLCN). Little is known about what FLCN does in a healthy individual and how best to treat those with BHD. As a first approach to developing a vertebrate model for BHD we aimed to identify the temporal and spatial expression of flcn transcripts in the developing zebrafish embryo. To gain insights into the function of flcn in a whole organism system we generated a loss of function model of flcn by the use of morpholino knockdown in zebrafish.

Results

flcn is expr

SUBMITTER: Kenyon EJ 

PROVIDER: S-EPMC4939010 | biostudies-literature | 2016 Jul

REPOSITORIES: biostudies-literature