TY - JOUR
T1 - Zebrafish ftz-f1 gene has two promoters, is alternatively spliced, and is expressed in digestive organs
AU - Lin, Wen Wen
AU - Wang, Hsin Wei
AU - Sum, Cristina
AU - Liu, Dong
AU - Hew, Choy L.
AU - Chung, Bon Chu
N1 - Copyright:
Copyright 2007 Elsevier B.V., All rights reserved.
PY - 2000/6/1
Y1 - 2000/6/1
N2 - Fushi-tarazu Factor-1 (FTZ-F1) is a family of nuclear receptors involved in various developmental processes. We have cloned a zebrafish FTZ-F1 gene, termed ff1, which belongs to the fetoprotein transcription factor/liver receptor homologue-1 (FTF/LRH-1) subgroup of the FTZ-F1 family. Four transcripts arise as a result of differential promoter usage and alternative splicing at the 3'-most exons. The longer transcript, form A, encodes a transcriptional activator. The shorter transcript, form B, lacks the activation domain, and hence could not activate transcription. The difference in promoter usage generates FF1 proteins with different N-terminal sequences. All four transcripts appear to be expressed in most of the adult tissues, whereas, during embryo development, the IIA form is the predominant transcript. Reverse transcriptase-PCR and in situ hybridization experiments showed that the ff1 transcript is expressed in the hypothalamus, spinal cord, mandibular arch and digestive organs, including pancreas. liver, and intestine. The expression of ff1 in the digestive organs implies its function in gut development.
AB - Fushi-tarazu Factor-1 (FTZ-F1) is a family of nuclear receptors involved in various developmental processes. We have cloned a zebrafish FTZ-F1 gene, termed ff1, which belongs to the fetoprotein transcription factor/liver receptor homologue-1 (FTF/LRH-1) subgroup of the FTZ-F1 family. Four transcripts arise as a result of differential promoter usage and alternative splicing at the 3'-most exons. The longer transcript, form A, encodes a transcriptional activator. The shorter transcript, form B, lacks the activation domain, and hence could not activate transcription. The difference in promoter usage generates FF1 proteins with different N-terminal sequences. All four transcripts appear to be expressed in most of the adult tissues, whereas, during embryo development, the IIA form is the predominant transcript. Reverse transcriptase-PCR and in situ hybridization experiments showed that the ff1 transcript is expressed in the hypothalamus, spinal cord, mandibular arch and digestive organs, including pancreas. liver, and intestine. The expression of ff1 in the digestive organs implies its function in gut development.
UR - http://www.scopus.com/inward/record.url?scp=0034213993&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0034213993&partnerID=8YFLogxK
U2 - 10.1042/0264-6021:3480439
DO - 10.1042/0264-6021:3480439
M3 - Article
C2 - 10816440
AN - SCOPUS:0034213993
SN - 0264-6021
VL - 348
SP - 439
EP - 446
JO - Biochemical Journal
JF - Biochemical Journal
IS - 2
ER -