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First published online 29 January 2003
doi: 10.1242/jcs.00272
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Research Article |
1 Integrated Program in Cellular, Molecular, and Biophysical Studies, Columbia
University College of Physicians and Surgeons, New York, NY 10032, USA
2 Department of Pathology, Columbia University College of Physicians and
Surgeons, New York, NY 10032, USA
3 Department of Anatomy and Cell Biology, Columbia University College of
Physicians and Surgeons, New York, NY 10032, USA
* Author for correspondence (e-mail: rkl2{at}columbia.edu)
Accepted 14 November 2002
The human Gas2-related gene on chromosome 22 (hGAR22)
encodes two alternatively spliced mRNA species. The longer mRNA encodes a
protein with a deduced molecular mass of 36.3 kDa (GAR22
), whereas the
shorter mRNA encodes a larger protein with a deduced molecular mass of 72.6
kDa (GAR22ß). We show that both hGAR22 proteins contain a calponin
homology actin-binding domain and a Gas2-related microtubule-binding domain.
Using rapid amplification of cDNA ends, we have cloned the mouse orthologue of
hGAR22, mGAR22, and found its protein products to be extremely well conserved.
We also report the cDNA cloning of a human Gas2-related gene on chromosome 17
(hGAR17). hGAR17 also encodes two protein isoforms. The overall
cytoskeletal binding properties of the hGAR17 and hGAR22 proteins are
remarkably similar. hGAR17 mRNA expression is limited to skeletal muscle.
Although hGAR22 and mGAR22 mRNAs are expressed nearly ubiquitously, mGAR22
protein can only be detected in testis and brain. Furthermore, only the ß
isoform is present in these tissues. GAR22ß expression is induced in a
variety of cultured cells by growth arrest. The absolute amounts of
GAR22ß protein expressed are low. The ß isoforms of hGAR17 and
hGAR22 appear to be able to crosslink microtubules and microfilaments in
transfected cells. This finding suggests that the physiological functions of
these proteins may involve integration of these two components of the
cytoskeleton.
Key words: Gas2, GAR17, GAR22, Microfilament, Microtubule
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