TY - JOUR
T1 - Identification of a novel adrenomedullin gene family in teleost fish
AU - Ogoshi, Maho
AU - Inoue, Koji
AU - Takei, Yoshio
N1 - Funding Information:
The authors thank Dr. Christopher A. Loretz of State University of New York for his critical reading of the manuscript. This work was supported in part by Grant-in-Aid for Creative Basic Research (12NP0201) from the Ministry of Education, Culture, Sports, Science and Technology of Japan, and for Scientific Research (13304063) from the Japan Society for the Promotion of Science to Y.T.
PY - 2003/11/28
Y1 - 2003/11/28
N2 - Adrenomedullin (AM) is a multifunctional peptide known to form a hormone family with calcitonin gene-related peptide (CGRP) and amylin. We have cloned five distinct AM cDNAs from the pufferfish, Takifugu rubripes, and named them TrAM-1, -2, -3, -4, and -5. Judging from the deduced precursor sequences and processing pattern of the C-terminal mature peptides, TrAMs may be divided into at least two groups; AM-2 and -3, and AM-1, -4, and possibly -5. Phylogenetic analysis of the mature peptides, exon-intron structure of their genes, and tissue distribution of their mRNA also support this classification. TrAM-1 and -4 were ubiquitously expressed in various tissues including the kidney and interrenal (adrenal homolog) as in the case of mammalian AM, while TrAM-2 and -3 were expressed most abundantly in the brain followed by the vascular tissues. Synteny of the genes around AM gene showed that TrAM-1 is the ortholog of mammalian AM. The presence of a PAMP-like sequence in the prosegment of TrAM-1 also supports this notion. Multiple AMs were also detected in another pufferfish, Tetraodon nigroviridis, and in zebrafish, Danio rerio. The present study shows for the first time the presence of a novel AM family in teleost fish that is independent from CGRP and amylin, which further suggests the possible existence of multiple AMs in mammals.
AB - Adrenomedullin (AM) is a multifunctional peptide known to form a hormone family with calcitonin gene-related peptide (CGRP) and amylin. We have cloned five distinct AM cDNAs from the pufferfish, Takifugu rubripes, and named them TrAM-1, -2, -3, -4, and -5. Judging from the deduced precursor sequences and processing pattern of the C-terminal mature peptides, TrAMs may be divided into at least two groups; AM-2 and -3, and AM-1, -4, and possibly -5. Phylogenetic analysis of the mature peptides, exon-intron structure of their genes, and tissue distribution of their mRNA also support this classification. TrAM-1 and -4 were ubiquitously expressed in various tissues including the kidney and interrenal (adrenal homolog) as in the case of mammalian AM, while TrAM-2 and -3 were expressed most abundantly in the brain followed by the vascular tissues. Synteny of the genes around AM gene showed that TrAM-1 is the ortholog of mammalian AM. The presence of a PAMP-like sequence in the prosegment of TrAM-1 also supports this notion. Multiple AMs were also detected in another pufferfish, Tetraodon nigroviridis, and in zebrafish, Danio rerio. The present study shows for the first time the presence of a novel AM family in teleost fish that is independent from CGRP and amylin, which further suggests the possible existence of multiple AMs in mammals.
KW - Adrenomedullin
KW - Comparative genomics
KW - Molecular evolution
KW - Pufferfish
KW - Takifugu rubripes
UR - http://www.scopus.com/inward/record.url?scp=0242521436&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0242521436&partnerID=8YFLogxK
U2 - 10.1016/j.bbrc.2003.10.111
DO - 10.1016/j.bbrc.2003.10.111
M3 - Article
C2 - 14623291
AN - SCOPUS:0242521436
SN - 0006-291X
VL - 311
SP - 1072
EP - 1077
JO - Biochemical and Biophysical Research Communications
JF - Biochemical and Biophysical Research Communications
IS - 4
ER -