Shinichiro Nishimatsu
   Department   Kawasaki Medical School  Kawasaki Medical School, Department of Natural Sciences,
   Position   Professor
Article types 原著
Language English
Peer review Peer reviewed
Title Isolation and characterization of two alternatively spliced complementary DNAs encoding a Xenopus laevis angiotensin II receptor.
Journal Formal name:Biochimica et biophysica acta
Abbreviation:Biochim Biophys Acta
ISSN code:00063002
Volume, Issue, Page 1218(3),pp.401-407
Author and coauthor Nishimatsu Shin-ichiro, Koyasu Naoko, Sugaya Takeshi, Ohnishi Junji, Yamagishi Toshiyuki, Murakami Kazuo, Miyazaki Hitoshi
Authorship Lead author
Publication date 1994/08
Summary We have isolated two cDNAs of 1.7 and 3.0 kb, produced by alternative splicing, that encode an angiotensin II (AII) receptor from a Xenopus laevis heart cDNA library. The two clones had identical coding regions with each other and were found to belong to the G protein-coupled receptor superfamily like the mammalian type 1 AII receptors (AT1); their amino acid sequence was 68.7% homologous with the human AT1 receptor sequence. However, there was a 1.3 kb insertion at the 3'-untranslated region of the longer clone. The insertion contained 9 repeats of an ATTTA motif, suggesting that the two mRNAs undergo distinct post-transcriptional regulation by virtue of a difference in their stability. Although the Xenopus receptor exhibited distinct specificities for AII receptor antagonists compared with mammalian AII receptors, several common characteristics, including the effect of dithiothreitol and guanosine 5'-O-(3-thiotriphosphate), demonstrated that the cloned receptor is a counterpart of the mammalian AT1 receptor. Moreover, the cloned receptor was expressed most abundantly in the Xenopus heart, which is inconsistent with the tissue distribution of mammalian AII receptors. This indicated that the Xenopus heart, unlike that of mammals, plays a major role in the AII-dependent regulation of blood pressure and extracellular fluid volume.
DOI 10.1016/0167-4781(94)90193-7
Document No. 7519446