TY - JOUR
T1 - Comparative analysis of human and mouse 3′ Igh regulatory regions identifies distinctive structural features
AU - Sepulveda, Manuel A.
AU - Garrett, Francine E.
AU - Price-Whelan, Alexa
AU - Birshtein, Barbara K.
N1 - Funding Information:
We thank Raju Kucherlapati (Department of Medicine, Harvard Medical School) for help with the screening of the RPCI-11 BAC library, Nasrin Ashouian and Eboni Benjamin for initial help with the Southern blots and BAC199M11 data analysis, Alexander Emelyanov and Sabrina Volpi for helpful discussions, and Bernice Morrow and Eric Bouhassira for critical review of the manuscript. This work was supported by an Albert Einstein Cancer Center grant P30CA1330, and NIH grants AI41572 and AI13509 to BKB. FG was supported by NCI 5F31 CA76942, UNCF/MERCK Graduate Science Research Dissertation Fellowship, and a National Medical Fellowship in Academic Medicine for Minority Medical Students.
PY - 2005/3
Y1 - 2005/3
N2 - Immunoglobulin heavy chain (Igh) locus rearrangements are controlled in part by an ∼30 kb complex 3′ regulatory region located 3′ of Cα: 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 ∼62 kb downstream of mouse Cα. 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) ∼120 kb downstream of mouse Cα. 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.
AB - Immunoglobulin heavy chain (Igh) locus rearrangements are controlled in part by an ∼30 kb complex 3′ regulatory region located 3′ of Cα: 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 ∼62 kb downstream of mouse Cα. 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) ∼120 kb downstream of mouse Cα. 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.
KW - 3′ Untranslated regions/immunology
KW - B-lymphocytes/immunology
KW - Conserved sequence
KW - Enhancer elements (genetics)/immunology
KW - Evolution
KW - Heavy-chain/genetics
KW - Immunoglobulins
KW - Molecular
KW - Molecular sequence data
KW - Nucleic acid
KW - Phylogeny
KW - Regulatory sequences
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U2 - 10.1016/j.molimm.2004.09.006
DO - 10.1016/j.molimm.2004.09.006
M3 - Article
C2 - 15607820
AN - SCOPUS:10844228012
SN - 0161-5890
VL - 42
SP - 605
EP - 615
JO - Immunochemistry
JF - Immunochemistry
IS - 5
ER -