Molecular cloning and sequencing of rat Cdc42 GTPase cDNA.
- Author:
Joong Soo HAN
1
;
Jong Hoon KIM
;
Jong Gon KIM
;
Jae Bong PARK
;
Dong Young NOH
;
Kweon Haeng LEE
Author Information
1. Institute of Biomedical Science and Department of Biochemistry, College of Medicine, Hanyang University, Seoul, Korea. jshan@email.hanyang.ac.kr
- Publication Type:Original Article ; Comparative Study ; Research Support, Non-U.S. Gov't
- Keywords:
GTPase;
Cdc42;
PCR Cloning;
COS-7 cell;
Rho
- MeSH:
Amino Acid Sequence;
Animal;
Base Sequence;
Cloning, Molecular;
Comparative Study;
Cross Reactions;
DNA, Complementary/genetics;
Human;
Molecular Sequence Data;
Rats;
Sequence Analysis, DNA;
Sequence Homology, Amino Acid;
cdc42 GTP-Binding Protein/immunology;
cdc42 GTP-Binding Protein/genetics*
- From:Experimental & Molecular Medicine
2000;32(3):115-119
- CountryRepublic of Korea
- Language:English
-
Abstract:
Cdc42 is a member of the Rho family of small GTP-ase and plays an important role in intracellular signaling pathways regulating cell morphology, motility and stimulation of DNA synthesis. We have isolated cDNA encoding Cdc42 from a rat brain cDNA library using PCR-cloning strategy. The sequence of isolated gene revealed an open reading frame of 576 nucleotides with the potential to encode a protein of 191 amino acids with a predicted molecular weight of 21 kD. The resulting sequence was incorporated into the GenBank with accession number, AF205635. Sequence analysis revealed that overall cDNA sequence identity is 96% with human G25K and 52% with rat Chp, a homologue of the GTPase human Cdc42Hs, and having one nucleotide difference from the mouse Cdc42. However, putative protein sequence was identical to the mouse and human brain Cdc42Hs. On expression of the cDNA in COS-7 cells, a protein molecular weight of 21 kD was detected in immunoblotting using anti-human Cdc42 antibodies. Therefore, these results suggest that the cDNA we are reporting is most likely the rat homologue of the GTPase human Cdc42.
