Genomic organization, promoter region analysis, and chromosome localization of the mouse bcl-x gene
- PMID: 9144489
Genomic organization, promoter region analysis, and chromosome localization of the mouse bcl-x gene
Abstract
The bcl-x gene, a bcl-2 family member, is highly regulated during lymphoid development, and its expression modulates apoptosis in lymphoid and other cell populations. Several forms of bcl-x mRNAs with different biologic functions have been described in rodents and humans. In this study, we have determined the organization and promoter region of the mouse bcl-x gene in an effort to understand the molecular basis for the different bcl-x mRNA species identified in tissues. We show that mouse bcl-x maps to the distal mouse chromosome 2 at approximately 89 cM, and exhibits a three-exon structure with an untranslated first exon and a facultative first intron. The coding region of bcl-xL is generated by the juncture of exons II and III through a splicing reaction, whereas bcl-xS is generated by an alternatively utilized donor splice site located within exon II. Analysis of multiple cDNAs and primer extension experiments revealed major transcription initiation sites in brain and thymus within a GC-rich region, with multiple Sp1-binding motifs located upstream of exon I. Another promoter was mapped to a 57-bp region localized upstream of the translation initiation codon by transfection of reporter constructs into FL5.12 and K562 cell lines. The remarkable similarity between the genomic regions of bcl-2 and bcl-x suggests that these genes have evolved from a common ancestral gene or through gene duplication.
Similar articles
-
Characterization and expression analyses of anti-apoptotic Bcl-2-like genes NR-13, Mcl-1, Bcl-X1, and Bcl-X2 in Atlantic cod (Gadus morhua).Mol Immunol. 2010 Jan;47(4):763-84. doi: 10.1016/j.molimm.2009.10.011. Epub 2009 Nov 17. Mol Immunol. 2010. PMID: 19923001
-
Transcriptional regulation of the mouse PNRC2 promoter by the nuclear factor Y (NFY) and E2F1.Gene. 2005 Nov 21;361:89-100. doi: 10.1016/j.gene.2005.07.012. Epub 2005 Sep 21. Gene. 2005. PMID: 16181749
-
ERF: genomic organization, chromosomal localization and promoter analysis of the human and mouse genes.Oncogene. 1997 Mar 27;14(12):1445-51. doi: 10.1038/sj.onc.1200965. Oncogene. 1997. PMID: 9136988
-
Genomic organization of the JEM-1 (BLZF1) gene on human chromosome 1q24: molecular cloning and analysis of its promoter region.Genomics. 2000 Nov 1;69(3):380-90. doi: 10.1006/geno.2000.6347. Genomics. 2000. PMID: 11056056
-
Mammalian glycosyltransferases: genomic organization and protein structure.Glycobiology. 1992 Aug;2(4):271-7. doi: 10.1093/glycob/2.4.271. Glycobiology. 1992. PMID: 1421748 Review.
Cited by
-
Sp1 and Sp3 are oxidative stress-inducible, antideath transcription factors in cortical neurons.J Neurosci. 2003 May 1;23(9):3597-606. doi: 10.1523/JNEUROSCI.23-09-03597.2003. J Neurosci. 2003. PMID: 12736330 Free PMC article.
-
Dexamethasone induces transcriptional activation of Bcl-xL gene and inhibits cardiac injury by myocardial ischemia.Eur J Pharmacol. 2011 Oct 1;668(1-2):194-200. doi: 10.1016/j.ejphar.2011.06.019. Epub 2011 Jun 25. Eur J Pharmacol. 2011. PMID: 21723861 Free PMC article.
-
Cantharidin induces apoptosis of human multiple myeloma cells via inhibition of the JAK/STAT pathway.Cancer Sci. 2008 Sep;99(9):1820-6. doi: 10.1111/j.1349-7006.2008.00872.x. Epub 2008 Jun 9. Cancer Sci. 2008. PMID: 18544087 Free PMC article.
-
Chronic Social Stress and Ethanol Increase Expression of KLF11, a Cell Death Mediator, in Rat Brain.Neurotox Res. 2015 Jul;28(1):18-31. doi: 10.1007/s12640-015-9524-1. Epub 2015 Mar 5. Neurotox Res. 2015. PMID: 25739536 Free PMC article.
-
Mechanisms of anthracycline cardiac injury: can we identify strategies for cardioprotection?Prog Cardiovasc Dis. 2010 Sep-Oct;53(2):105-13. doi: 10.1016/j.pcad.2010.06.007. Prog Cardiovasc Dis. 2010. PMID: 20728697 Free PMC article. Review.
Publication types
MeSH terms
Substances
Associated data
- Actions
- Actions
Grants and funding
LinkOut - more resources
Other Literature Sources
Molecular Biology Databases
Research Materials
Miscellaneous