TY - JOUR
T1 - cDNA cloning of Na+, K+-ATPase α-subunit from embryos of the sea urchin, Hemicentrotus pulcherrimus
AU - Mitsunaga-Nakatsubo, Keiko
AU - Yamazaki, Ken
AU - Hatoh-Okazaki, Midori
AU - Kawashita, Hiroto
AU - Okamura, Chisato
AU - Akasaka, Koji
AU - Shimada, Hiraku
AU - Yasumasu, Ikuo
N1 - Copyright:
Copyright 2018 Elsevier B.V., All rights reserved.
PY - 1996/12
Y1 - 1996/12
N2 - Na+, K+-ATPase α-subunit cDNA of the sea urchin, Hemicentrotus pulcherrimus, was obtained by twice screening prism and gastrula λgt10 cDNA libraries using an oligonucleotide probe derived from a mostly conserved region, FSBA (5′-p-(fluorosulfonyl)-benzoyladenosine) binding site of cation transport ATPases. The 5′-end of the non-coding region was determined by primer extension and the region was amplified by 5′-RACE method. The sea urchin α-subunit cDNA consists of 4401 nucleotides and encodes 1038 amino acid residues (MW, 114 kDa). The predicted primary structure, except N-terminal region, has similar degree of high homology to various metazoan Na+, K+-ATPase α-subunits. Alignment of amino acid sequence and a hydropathy profile also predicts eight putative transmembrane segments at least. The phylogenetic tree suspected from alignment of amino acid sequences of 21 species suggests that sea urchin and vertebrate Na+, K+-ATPase α-subunits seem to have evolved from a common origin, before vertebrate α-subunit divided into three isoforms.
AB - Na+, K+-ATPase α-subunit cDNA of the sea urchin, Hemicentrotus pulcherrimus, was obtained by twice screening prism and gastrula λgt10 cDNA libraries using an oligonucleotide probe derived from a mostly conserved region, FSBA (5′-p-(fluorosulfonyl)-benzoyladenosine) binding site of cation transport ATPases. The 5′-end of the non-coding region was determined by primer extension and the region was amplified by 5′-RACE method. The sea urchin α-subunit cDNA consists of 4401 nucleotides and encodes 1038 amino acid residues (MW, 114 kDa). The predicted primary structure, except N-terminal region, has similar degree of high homology to various metazoan Na+, K+-ATPase α-subunits. Alignment of amino acid sequence and a hydropathy profile also predicts eight putative transmembrane segments at least. The phylogenetic tree suspected from alignment of amino acid sequences of 21 species suggests that sea urchin and vertebrate Na+, K+-ATPase α-subunits seem to have evolved from a common origin, before vertebrate α-subunit divided into three isoforms.
UR - http://www.scopus.com/inward/record.url?scp=0030437263&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0030437263&partnerID=8YFLogxK
U2 - 10.2108/zsj.13.833
DO - 10.2108/zsj.13.833
M3 - Article
C2 - 9107140
AN - SCOPUS:0030437263
SN - 0289-0003
VL - 13
SP - 833
EP - 841
JO - Zoological Science
JF - Zoological Science
IS - 6
ER -