Skip to main content

Thank you for visiting nature.com. You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript.

Advertisement

Experimental & Molecular Medicine
  • View all journals
  • Search
  • My Account Login
  • Content Explore content
  • About the journal
  • Publish with us
  • Sign up for alerts
  • RSS feed
  1. nature
  2. experimental & molecular medicine
  3. articles
  4. article
Molecular cloning and sequencing of rat Cdc42 GTPase cDNA
Download PDF
Download PDF
  • Article
  • Open access
  • Published: 01 September 2000

Molecular cloning and sequencing of rat Cdc42 GTPase cDNA

  • Joong-Soo Han1,
  • Jong-Hoon Kim,
  • Jong Gon Kim,
  • Jae-Bong Park,
  • Dong-Young Noh &
  • …
  • Kweon-Haeng Lee 

Experimental & Molecular Medicine volume 32, pages 115–119 (2000)Cite this article

  • 589 Accesses

  • Metrics details

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.

Similar content being viewed by others

Efficient genetic code expansion without host genome modifications

Article 11 September 2024

Validated assays for the quantification of C9orf72 human pathology

Article Open access 08 January 2024

Patterning of the cell cortex by Rho GTPases

Article 03 January 2024

Article PDF

Author information

Authors and Affiliations

  1. Institute of Biomedical Science and Department of Biochemistry, College of Medicine, Hanyang University, Seoul, Korea

    Joong-Soo Han

Authors
  1. Joong-Soo Han
    View author publications

    Search author on:PubMed Google Scholar

  2. Jong-Hoon Kim
    View author publications

    Search author on:PubMed Google Scholar

  3. Jong Gon Kim
    View author publications

    Search author on:PubMed Google Scholar

  4. Jae-Bong Park
    View author publications

    Search author on:PubMed Google Scholar

  5. Dong-Young Noh
    View author publications

    Search author on:PubMed Google Scholar

  6. Kweon-Haeng Lee
    View author publications

    Search author on:PubMed Google Scholar

Rights and permissions

This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

Reprints and permissions

About this article

Cite this article

Han, JS., Kim, JH., Kim, J. et al. Molecular cloning and sequencing of rat Cdc42 GTPase cDNA. Exp Mol Med 32, 115–119 (2000). https://doi.org/10.1038/emm.2000.20

Download citation

  • Published: 01 September 2000

  • Issue date: 01 September 2000

  • DOI: https://doi.org/10.1038/emm.2000.20

Share this article

Anyone you share the following link with will be able to read this content:

Sorry, a shareable link is not currently available for this article.

Provided by the Springer Nature SharedIt content-sharing initiative

Keywords

  • GTPase
  • Cdc42
  • PCR Cloning
  • COS-7 cell
  • Rho
Download PDF

Advertisement

Explore content

  • Research articles
  • Reviews & Analysis
  • News & Comment
  • Current issue
  • Collections
  • Sign up for alerts
  • RSS feed

About the journal

  • Special Feature
  • Journal Information
  • About the Editors
  • About the Partner
  • Contact
  • For Advertisers
  • Press Releases
  • Open Access Fees and Funding

Publish with us

  • For Authors & Referees
  • Language editing services
  • Submit manuscript

Search

Advanced search

Quick links

  • Explore articles by subject
  • Find a job
  • Guide to authors
  • Editorial policies

Experimental & Molecular Medicine (Exp Mol Med)

ISSN 2092-6413 (online)

ISSN 1226-3613 (print)

nature.com sitemap

About Nature Portfolio

  • About us
  • Press releases
  • Press office
  • Contact us

Discover content

  • Journals A-Z
  • Articles by subject
  • protocols.io
  • Nature Index

Publishing policies

  • Nature portfolio policies
  • Open access

Author & Researcher services

  • Reprints & permissions
  • Research data
  • Language editing
  • Scientific editing
  • Nature Masterclasses
  • Research Solutions

Libraries & institutions

  • Librarian service & tools
  • Librarian portal
  • Open research
  • Recommend to library

Advertising & partnerships

  • Advertising
  • Partnerships & Services
  • Media kits
  • Branded content

Professional development

  • Nature Awards
  • Nature Careers
  • Nature Conferences

Regional websites

  • Nature Africa
  • Nature China
  • Nature India
  • Nature Japan
  • Nature Middle East
  • Privacy Policy
  • Use of cookies
  • Legal notice
  • Accessibility statement
  • Terms & Conditions
  • Your US state privacy rights
Springer Nature

© 2025 Springer Nature Limited