TY - JOUR
T1 - Identification of a novel splicing form of zebrafish p73 having a strong transcriptional activity
AU - Satoh, Shinya
AU - Arai, Ken Ichi
AU - Watanabe, Sumiko
N1 - Funding Information:
We thank C. Nakata and R. Kurita for general discussions, and Y. Matsumura for secretarial help. This work was supported by the RIKEN Center for Developmental Biology.
PY - 2004/12/17
Y1 - 2004/12/17
N2 - p73 is a transcriptional activator related to tumor suppressor p53 and regulates differentiation, cell-cycle arrest, and apoptosis. Recently, zebrafish p73 (zp73α) was isolated and shown to be required for zebrafish embryogenesis. In this study, we isolated a novel splicing-variant of zp73 mRNA, which was generated by the use of an alternative splicing acceptor site, and designated it as zp73θ. The zp73θ mRNA encoded a carboxy-terminal structure distinct from that of zp73α. Whereas the expression level of zp73θ mRNA was much lower than that of zp73α in zebrafish adult tissues, it was relatively high and fluctuated during embryogenesis. Using Saos-2 cells for a transient reporter assay, we found that zp73θ, but not zp73α, had strong transcriptional activity when the experiments were performed at 34°C. In addition, zp73θ had the ability to suppress the growth of Saos-2 cells and to cause the developmental defects in zebrafish. These data indicated that zp73θ could work as a transcriptional activator in zebrafish.
AB - p73 is a transcriptional activator related to tumor suppressor p53 and regulates differentiation, cell-cycle arrest, and apoptosis. Recently, zebrafish p73 (zp73α) was isolated and shown to be required for zebrafish embryogenesis. In this study, we isolated a novel splicing-variant of zp73 mRNA, which was generated by the use of an alternative splicing acceptor site, and designated it as zp73θ. The zp73θ mRNA encoded a carboxy-terminal structure distinct from that of zp73α. Whereas the expression level of zp73θ mRNA was much lower than that of zp73α in zebrafish adult tissues, it was relatively high and fluctuated during embryogenesis. Using Saos-2 cells for a transient reporter assay, we found that zp73θ, but not zp73α, had strong transcriptional activity when the experiments were performed at 34°C. In addition, zp73θ had the ability to suppress the growth of Saos-2 cells and to cause the developmental defects in zebrafish. These data indicated that zp73θ could work as a transcriptional activator in zebrafish.
KW - Alternative splicing
KW - Transcriptional activity
KW - Zebrafish
KW - p73
UR - http://www.scopus.com/inward/record.url?scp=8444249597&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=8444249597&partnerID=8YFLogxK
U2 - 10.1016/j.bbrc.2004.10.109
DO - 10.1016/j.bbrc.2004.10.109
M3 - Article
C2 - 15541366
AN - SCOPUS:8444249597
SN - 0006-291X
VL - 325
SP - 835
EP - 842
JO - Biochemical and Biophysical Research Communications
JF - Biochemical and Biophysical Research Communications
IS - 3
ER -