Published November 26, 2004 | Version v1
Journal article

Identification and characterization of a lymphocytic Rho-GTPase effector: rhotekin-2

  • 1. Douglas Hocking Research Institute, Barwon Health, Geelong Hospital, Geelong, Vic. 3220 (Australia) and Metabolic Research Unit, School of Health Sciences, Deakin University, Geelong, Vic. 3216 (Australia)
  • 2. Douglas Hocking Research Institute, Barwon Health, Geelong Hospital, Geelong, Vic. 3220 (Australia)
  • 3. Metabolic Research Unit, School of Health Sciences, Deakin University, Geelong, Vic. 3216 (Australia)

Description

Rhotekin belongs to the group of proteins containing a Rho-binding domain that are target peptides (effectors) for the Rho-GTPases. We previously identified a novel cDNA with homology to human rhotekin and in this study we cloned and characterized the coding region of this novel 12-exon gene. The ORF encodes a 609 amino-acid protein comprising a Class I Rho-binding domain and pleckstrin homology (PH) domain. Cellular cDNA expression of this new protein, designated Rhotekin-2 (RTKN2), was shown in the cytosol and nucleus of CHO cells. Using bioinformatics and RTPCR we identified three major splice variants, which vary in both the Rho-binding and PH domains. Real-time PCR studies showed exclusive RTKN2 expression in pooled lymphocytes and further purification indicated sole expression in CD4pos T-cells and bone marrow-derived B-cells. Gene expression was increased in quiescent T-cells but negligible in activated proliferating cells. In malignant samples expression was absent in myeloid leukaemias, low in most B-cell malignancies and CD8pos T-cell malignancies, but very high in CD4pos/CD8pos T-lymphoblastic lymphoma. As the Rho family is critical in lymphocyte development and function, RTKN2 may play an important role in lymphopoiesis

Additional details

Identifiers

DOI
10.1016/j.bbrc.2004.09.205;
PII
S0006-291X(04)02253-3;

Publishing Information

Journal Title
Biochemical and Biophysical Research Communications
Journal Volume
324
Journal Issue
4
Journal Page Range
p. 1360-1369
ISSN
0006-291X
CODEN
BBRCA9

Optional Information

Copyright
Copyright (c) 2004 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.