KH domain integrity is required for wild-type localization of Sam68 - PubMed
- ️Thu Jan 01 1998
. 1998 May 25;241(1):84-95.
doi: 10.1006/excr.1998.4047.
Affiliations
- PMID: 9633516
- DOI: 10.1006/excr.1998.4047
Free article
KH domain integrity is required for wild-type localization of Sam68
A E McBride et al. Exp Cell Res. 1998.
Free article
Abstract
The protein Sam68 (Src-associated in mitosis, 68 kDa) has been found to bind to SH2 and to SH3 domain-containing proteins and to RNA. Although its protein-protein interactions implicate Sam68 in cell signaling, the significance of its RNA binding remains obscure. In most cells, Sam68 shows diffuse nucleoplasmic staining. Upon treatment with transcription inhibitors, however, Sam68 localize into punctate nuclear structures. Mutant forms of mouse Sam68 were overexpressed in human cells to test the importance of the KH domain, which is required for RNA binding, in the intracellular localization of Sam68. A small deletion within the KH domain (delta 206-218) or point mutation I184N had no effect upon the localization of overexpressed Sam68. Sam68 that contained a deletion of the entire KH domain (delta KH, delta 157-256) or point mutation G178E, however, localized to distinct nuclear spots. Furthermore, delta KH Sam68, unlike wild-type Sam68 and several other mutant Sam68 proteins, did not relocalize upon poliovirus infection and caused the normally cytoplasmic viral polymerase to localize to the nuclear spots. Thus both ongoing transcription and an intact KH domain are crucial determinants of the dynamic intracellular localization of Sam68.
Similar articles
-
Evidence for SH3 domain directed binding and phosphorylation of Sam68 by Src.
Shen Z, Batzer A, Koehler JA, Polakis P, Schlessinger J, Lydon NB, Moran MF. Shen Z, et al. Oncogene. 1999 Aug 19;18(33):4647-53. doi: 10.1038/sj.onc.1203079. Oncogene. 1999. PMID: 10467411
-
Hong W, Resnick RJ, Rakowski C, Shalloway D, Taylor SJ, Blobel GA. Hong W, et al. Mol Cancer Res. 2002 Nov;1(1):48-55. Mol Cancer Res. 2002. PMID: 12496368
-
Reaching for the stars: Linking RNA binding proteins to diseases.
Richard S. Richard S. Adv Exp Med Biol. 2010;693:142-57. Adv Exp Med Biol. 2010. PMID: 21189691 Review.
-
Targeting the RNA-binding protein Sam68 as a treatment for cancer?
Lukong KE, Richard S. Lukong KE, et al. Future Oncol. 2007 Oct;3(5):539-44. doi: 10.2217/14796694.3.5.539. Future Oncol. 2007. PMID: 17927519 Review.
Cited by
-
Coyle JH, Guzik BW, Bor YC, Jin L, Eisner-Smerage L, Taylor SJ, Rekosh D, Hammarskjöld ML. Coyle JH, et al. Mol Cell Biol. 2003 Jan;23(1):92-103. doi: 10.1128/MCB.23.1.92-103.2003. Mol Cell Biol. 2003. PMID: 12482964 Free PMC article.
-
The multifaceted poliovirus 2A protease: regulation of gene expression by picornavirus proteases.
Castelló A, Alvarez E, Carrasco L. Castelló A, et al. J Biomed Biotechnol. 2011;2011:369648. doi: 10.1155/2011/369648. Epub 2011 Apr 14. J Biomed Biotechnol. 2011. PMID: 21541224 Free PMC article.
-
Sam68 exerts separable effects on cell cycle progression and apoptosis.
Taylor SJ, Resnick RJ, Shalloway D. Taylor SJ, et al. BMC Cell Biol. 2004 Jan 22;5:5. doi: 10.1186/1471-2121-5-5. BMC Cell Biol. 2004. PMID: 14736338 Free PMC article.
-
A role for the GSG domain in localizing Sam68 to novel nuclear structures in cancer cell lines.
Chen T, Boisvert FM, Bazett-Jones DP, Richard S. Chen T, et al. Mol Biol Cell. 1999 Sep;10(9):3015-33. doi: 10.1091/mbc.10.9.3015. Mol Biol Cell. 1999. PMID: 10473643 Free PMC article.
-
Henao-Mejia J, He JJ. Henao-Mejia J, et al. Exp Cell Res. 2009 Nov 15;315(19):3381-95. doi: 10.1016/j.yexcr.2009.07.011. Epub 2009 Jul 14. Exp Cell Res. 2009. PMID: 19615357 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Miscellaneous