HUMAN-JK RECOMBINATION SIGNAL BINDING-PROTEIN GENE (IGKJRB) - COMPARISON WITH ITS MOUSE HOMOLOG

被引:57
作者
AMAKAWA, R
JING, W
OZAWA, K
MATSUNAMI, N
HAMAGUCHI, Y
MATSUDA, F
KAWAICHI, M
HONJO, T
机构
[1] KYOTO UNIV,DEPT MED CHEM,SAKYO KU,KYOTO 606,JAPAN
[2] KYOTO UNIV,FAC MED,DEPT INTERNAL MED 1,SAKYO KU,KYOTO 606,JAPAN
[3] KYOTO UNIV,CTR MOLEC BIOL & GENET,SAKYO KU,KYOTO 606,JAPAN
[4] INST PHYS & CHEM RES,TSUKUBA LIFE SCI CTR,GENE BANK,WAKO,SAITAMA 351,JAPAN
关键词
D O I
10.1006/geno.1993.1326
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The mouse Igkjrb protein specifically binds to the immunoglobulin Jk recombination signal sequence. The IGKJRB gene is highly conserved among many species such as human, Xenopus, and Drosophila. Using cDNA fragments of the mouse Igkjrb gene, we isolated its human counterpart, IGKJRB. The human genome contains one functional IGKJRB gene and two types of processed pseudogenes. In situ chromosome hybridization analysis demonstrated that the functional gene is localized at chromosome 3q25, and the pseudogenes (IGKJRBP1 and IGKJRBP2, respectively) are located at chromosomes 9p13 and 9q13. The functional gene is composed of 13 exons spanning at least 67 kb. Three types of cDNA with different 5′ sequences were isolated by rapid amplification of cDNA ends, suggesting the presence of three proteins. The aPCR-1 protein, which possessed the exon 1 sequence, was the counterpart of the mouse RBP-2 type protein. The aPCR-2 and 3 proteins may be specific to human cells because the mouse counterparts were not detected. The amino acid sequences of the human and mouse IGKJRB genes were 98% homologous in exons 2-11, whereas the homology of the human and mouse exon 1 sequences was 75%. © 1993 Academic Press. All rights reserved.
引用
收藏
页码:306 / 315
页数:10
相关论文
共 40 条
  • [1] 2 PAIRS OF RECOMBINATION SIGNALS ARE SUFFICIENT TO CAUSE IMMUNOGLOBULIN-V-(D)-J JOINING
    AKIRA, S
    OKAZAKI, K
    SAKANO, H
    [J]. SCIENCE, 1987, 238 (4830) : 1134 - 1138
  • [2] ORGANIZATION AND REORGANIZATION OF IMMUNOGLOBULIN GENES IN A-MULV TRANSFORMED-CELLS - REARRANGEMENT OF HEAVY BUT NOT LIGHT CHAIN GENES
    ALT, F
    ROSENBERG, N
    LEWIS, S
    THOMAS, E
    BALTIMORE, D
    [J]. CELL, 1981, 27 (02) : 381 - 390
  • [3] AMAKAWA R, 1990, CANCER RES, V50, P2423
  • [4] THE INTEGRASE FAMILY OF SITE-SPECIFIC RECOMBINASES - REGIONAL SIMILARITIES AND GLOBAL DIVERSITY
    ARGOS, P
    LANDY, A
    ABREMSKI, K
    EGAN, JB
    HAGGARDLJUNGQUIST, E
    HOESS, RH
    KAHN, ML
    KALIONIS, B
    NARAYANA, SVL
    PIERSON, LS
    STERNBERG, N
    LEONG, JM
    [J]. EMBO JOURNAL, 1986, 5 (02) : 433 - 440
  • [6] DYSTROPHIN IS TRANSCRIBED IN BRAIN FROM A DISTANT UPSTREAM PROMOTER
    BOYCE, FM
    BEGGS, AH
    FEENER, C
    KUNKEL, LM
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (04) : 1276 - 1280
  • [7] ISOLATION OF BIOLOGICALLY-ACTIVE RIBONUCLEIC-ACID FROM SOURCES ENRICHED IN RIBONUCLEASE
    CHIRGWIN, JM
    PRZYBYLA, AE
    MACDONALD, RJ
    RUTTER, WJ
    [J]. BIOCHEMISTRY, 1979, 18 (24) : 5294 - 5299
  • [8] CRAIG NL, 1988, ANNU REV GENET, V22, P77
  • [9] A TECHNIQUE FOR RADIOLABELING DNA RESTRICTION ENDONUCLEASE FRAGMENTS TO HIGH SPECIFIC ACTIVITY
    FEINBERG, AP
    VOGELSTEIN, B
    [J]. ANALYTICAL BIOCHEMISTRY, 1983, 132 (01) : 6 - 13
  • [10] FROHMAN MA, 1988, P NATL ACAD SCI USA, V85, P8988