Journal
MOLECULAR IMMUNOLOGY
Volume 42, Issue 5, Pages 605-615Publisher
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.molimm.2004.09.006
Keywords
3' untranslated regions/immunology; B-lymphocytes/immunology; enhancer elements (genetics)/immunology; immunoglobulins; heavychain/genetics; regulatory sequences; nucleic acid; molecular sequence data; conserved sequence; phylogeny; evolution; molecular; human; mice; rats
Categories
Funding
- NCI NIH HHS [5F31 CA76942, P30CA1330] Funding Source: Medline
- NIAID NIH HHS [R01 AI013509-27A2, AI41572, AI13509] Funding Source: Medline
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Immunoglobulin heavy chain (Igh) locus rearrangements are controlled in part by an similar to 30 kb complex 3 ' regulatory region located 3 ' of C alpha: this region contains several enhancers. We report here the comparison of the genomic sequences of the 3 ' regulatory region and further downstream sequences from mouse, rat, human and chimpanzee. Only short segments of homology were detected in the 3 ' regulatory region, and these were located in the vicinity of the known 3 ' enhancers. The nearest highly conserved segment is the nearest non-Igh gene, hole, which is located similar to 62 kb downstream of mouse Cut. Analysis of murine 3 ' Igh sequences by single nucleotide polymorphism (SNP) and restriction fragment length polymorphism (RFLP) detected a transition region (high to low SNP or RFLP density) similar to 120 kb downstream of mouse C alpha. Although there is only limited sequence identity between rodent and primate 3 ' Igh regulatory regions, all of these regulatory regions contain a palindrome and locally repetitive elements. Locally repetitive elements in primates comprise blocks of switch-like sequences that differ from the families of inverted and tandem repeats that are present in rodents. We propose that together with enhancers, these conserved structural features are essential for the activity of the 3 ' Igh regulatory region in vivo. (c) 2004 Elsevier Ltd. All rights reserved.
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