TY - JOUR
T1 - Occurrence of pre-MBT synthesis of caspase-8 mRNA and activation of caspase-8 prior to execution of SAMDC (S-adenosylmethionine decarboxylase)- induced, but not p53-induced, apoptosis in Xenopus late blastulae
AU - Shiokawa, Koichiro
AU - Takayama, Eiji
AU - Higo, Takayasu
AU - Kuroyanagi, Shinsaku
AU - Kaito, Chikara
AU - Hara, Hiroshi
AU - Kajitani, Masayuki
AU - Sekimizu, Kazuhisa
AU - Tadakuma, Takushi
AU - Miura, Kin Ichiro
AU - Igarashi, Kazuei
AU - Yaoita, Yoshio
N1 - Funding Information:
The present work was supported, in part, by a grant from Magnetic Health Science Foundation (Japan) (2004 recipient; K.S.) and presentation by K.S. of some of these results at 2005 Gordon Conference (Polyamines) in Connecticut College was supported by The Naito Foundation. The authors thank Dr. K. Nakajima for technical helps about caspase plasmids. The authors also thank Ms. M. Ohara for editing services.
PY - 2005/10/21
Y1 - 2005/10/21
N2 - Overexpression of S-adenosylmethionine decarboxylase (SAMDC) in Xenopus fertilized eggs activates caspase-9 and executes maternal program of apoptosis shortly after midblastula transition (MBT). We find that overexpression of caspase-8 and p53, like that of SAMDC, induces apoptosis in Xenopus late blastulae. The apoptosis induced by p53 was abolished by injection of mRNA for xdm-2, a negative regulator of p53, and by injection of a peptide inhibitor or a dominant-negative type mutant of caspase-9, but not caspase-8. The apoptosis induced by SAMDC was not abolished by injection of xdm-2 mRNA, but was abolished by injection of a peptide inhibitor or a dominant-negative type mutant mRNA of both caspase-9 and caspase-8. Unlike caspase-9 mRNA, caspase-8 mRNA did not occur as a maternal mRNA rather induced to be expressed during cleavage stage (pre-MBT stage) by overexpression of SAMDC but not p53. Furthermore, while activities to process procaspase-8 and procaspase-9 appeared in SAMDC-overexpressed apoptotic embryos, the activity to process procaspase-8 did not appear in p53-overexpressed apoptotic embryos. We conclude there are at least two pathways in the execution of the maternal program of apoptosis in Xenopus embryos; one being through do novo expression of caspase-8 gene during cleavage stage, and the other without involvement of caspase-8.
AB - Overexpression of S-adenosylmethionine decarboxylase (SAMDC) in Xenopus fertilized eggs activates caspase-9 and executes maternal program of apoptosis shortly after midblastula transition (MBT). We find that overexpression of caspase-8 and p53, like that of SAMDC, induces apoptosis in Xenopus late blastulae. The apoptosis induced by p53 was abolished by injection of mRNA for xdm-2, a negative regulator of p53, and by injection of a peptide inhibitor or a dominant-negative type mutant of caspase-9, but not caspase-8. The apoptosis induced by SAMDC was not abolished by injection of xdm-2 mRNA, but was abolished by injection of a peptide inhibitor or a dominant-negative type mutant mRNA of both caspase-9 and caspase-8. Unlike caspase-9 mRNA, caspase-8 mRNA did not occur as a maternal mRNA rather induced to be expressed during cleavage stage (pre-MBT stage) by overexpression of SAMDC but not p53. Furthermore, while activities to process procaspase-8 and procaspase-9 appeared in SAMDC-overexpressed apoptotic embryos, the activity to process procaspase-8 did not appear in p53-overexpressed apoptotic embryos. We conclude there are at least two pathways in the execution of the maternal program of apoptosis in Xenopus embryos; one being through do novo expression of caspase-8 gene during cleavage stage, and the other without involvement of caspase-8.
KW - Caspase-8
KW - Caspase-9
KW - Dominant-negative caspases
KW - Maternal program of apoptosis
KW - Overexpression of SAMDC
KW - Pre-MBT transcription
KW - Xdm-2
KW - Xenopus laevis embryos
KW - p53
UR - http://www.scopus.com/inward/record.url?scp=24644485373&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=24644485373&partnerID=8YFLogxK
U2 - 10.1016/j.bbrc.2005.08.144
DO - 10.1016/j.bbrc.2005.08.144
M3 - Article
C2 - 16143307
AN - SCOPUS:24644485373
SN - 0006-291X
VL - 336
SP - 682
EP - 691
JO - Biochemical and Biophysical Research Communications
JF - Biochemical and Biophysical Research Communications
IS - 2
ER -