Genomic structure and chromosomal localization of processed pseudogenes for human RBP-Jk
- 1 December 1994
- journal article
- research article
- Published by Springer Nature in Journal of Human Genetics
- Vol. 39 (4), 393-401
- https://doi.org/10.1007/bf01892384
Abstract
The functional gene for human recombination signal sequence-binding protein (RBP-Jk) and corresponding processed psudogenes have been isolated from various species, such asDrosophila, Xenopus, mouse, and human. Here we report the isolation of another two genomic pseudogenes of human RBP-Jk, named K2 and K7, from a cosmid library of Hela cells. The nucleotide sequences of both genes exhibited more than 95% homology to the functional human gene for RBP-Jk. Moreover, they did not contain any intron sequences and were interrupted by several stop codons in all frames.In situ hybridization demonstrated that the pseudogenes, K2 and K7, were localized at chromosomes 9p13 and 9q13, respectively. Their physical maps differed from those of the true functional gene and of the pseudogenes reported previously by Amakawaet al. (1993).Keywords
This publication has 19 references indexed in Scilit:
- A mathematically designed STS primer without any mismatches for direct sequencing of cosmid DNA clonesJournal of Human Genetics, 1993
- The Drosophila homolog of the immunoglobulin recombination signal-binding protein regulates peripheral nervous system developmentCell, 1992
- RAG-2-deficient mice lack mature lymphocytes owing to inability to initiate V(D)J rearrangementCell, 1992
- RAG-1-deficient mice have no mature B and T lymphocytesCell, 1992
- The scid mutation in mice causes a general defect in DNA repairNature, 1990
- High-Resolution Mapping of Human Chromosome 11 by in Situ Hybridization with Cosmid ClonesScience, 1990
- A protein binding to the Jk recombination sequence of immunoglobulin genes contains a sequence related to the integrase motifNature, 1989
- The defect in murine severe combined immune deficiency: Joining of signal sequences but not coding segments in V(D)J recombinationCell, 1988
- ORIGIN OF IMMUNE DIVERSITY: GENETIC VARIATION AND SELECTIONAnnual Review of Biochemistry, 1985
- Somatic generation of antibody diversityNature, 1983