Genomic organization of the gene coding for TIRC7, a novel membrane protein essential for T cell activation

被引:64
作者
Heinemann, T
Bulwin, GC
Randall, J
Schnieders, B
Sandhoff, K
Volk, HD
Milford, E
Gullans, SR
Utku, N [1 ]
机构
[1] Univ Bonn, Kekule Inst Organ Chem & Biochem, D-53121 Bonn, Germany
[2] Humboldt Univ, Inst Med Immunol, D-10098 Berlin, Germany
[3] Univ Cologne, Inst Med Mikrobiol & Hyg, D-50924 Cologne, Germany
[4] Harvard Univ, Sch Med, Harvard Inst Med, Boston, MA 02115 USA
[5] Brigham & Womens Hosp, Dept Med, Div Renal, Boston, MA 02115 USA
关键词
D O I
10.1006/geno.1999.5751
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
A novel human membrane protein, TIRC7, was recently identified and demonstrated to be essential in T cell activation. Here we report on the genomic organization of the TIRC7 gene, which is composed of 15 exons and spans 7.9 kb, The seven predicted transmembrane-spanning domains of the TIRC7 protein coincide well with exon-intron boundaries, TIRC7 and OC116, a recently described putative subunit of the vacuolar proton pump that was demonstrated to be expressed in an osteoclastoma tumor as well. as in a human pancreatic adenocarcinoma cell line, are demonstrated to be alternative transcripts of the same gene. OC116 consists of 20 exons with the last 14 introns and exons being identical with those of TIRC7. The chromosomal locus for both transcripts was identified on chromosome 11q13.4-q13.5. In human alloactivated T lymphocytes, mRNA expression of TIRC7, but not OC116, is demonstrated, indicating that OC116 is not involved in regular T cell proliferation, (C) 1999 Academic Press.
引用
收藏
页码:398 / 406
页数:9
相关论文
共 26 条
  • [1] Distinct roles for LFA-1 and CD28 during activation of naive T cells: Adhesion versus costimulation
    Bachmann, MF
    McKallFaienza, K
    Schmits, R
    Bouchard, D
    Beach, J
    Speiser, DE
    Mak, TW
    Ohashi, PS
    [J]. IMMUNITY, 1997, 7 (04) : 549 - 557
  • [2] F-19-NMR STUDY OF PRIMARY HUMAN T-LYMPHOCYTE ACTIVATION - EFFECTS OF MITOGEN ON INTRACELLULAR PH
    BENTAL, M
    DEUTSCH, C
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY, 1994, 266 (02): : C541 - C551
  • [3] BOWMAN EJ, 1988, J BIOL CHEM, V263, P13994
  • [4] Positional cloning of the gene for multiple endocrine neoplasia-type 1
    Chandrasekharappa, SC
    Guru, SC
    Manickam, P
    Olufemi, SE
    Collins, FS
    EmmertBuck, MR
    Debelenko, LV
    Zhuang, ZP
    Lubensky, IA
    Liotta, LA
    Crabtree, JS
    Wang, YP
    Roe, BA
    Weisemann, J
    Boguski, MS
    Agarwal, SK
    Kester, MB
    Kim, YS
    Heppner, C
    Dong, QH
    Spiegel, AM
    Burns, AL
    Marx, SJ
    [J]. SCIENCE, 1997, 276 (5311) : 404 - 407
  • [5] CONTINGENT GENETIC REGULATORY EVENTS IN LYMPHOCYTE-T ACTIVATION
    CRABTREE, GR
    [J]. SCIENCE, 1989, 243 (4889) : 355 - 361
  • [6] The vacuolar H+-ATPase: A universal proton pump of eukaryotes
    Finbow, ME
    Harrison, MA
    [J]. BIOCHEMICAL JOURNAL, 1997, 324 : 697 - 712
  • [7] Physiology and biochemistry of the kidney vacuolar H+-ATPase
    Gluck, SL
    Underhill, DM
    Iyori, M
    Holliday, LS
    Kostrominova, TY
    Lee, BS
    [J]. ANNUAL REVIEW OF PHYSIOLOGY, 1996, 58 : 427 - 445
  • [8] CELL ACIDIFICATION IN APOPTOSIS - GRANULOCYTE-COLONY-STIMULATING FACTOR DELAYS PROGRAMMED CELL-DEATH IN NEUTROPHILS BY UP-REGULATING THE VACUOLAR H+-ATPASE
    GOTTLIEB, RA
    GIESING, HA
    ZHU, JY
    ENGLER, RL
    BABIOR, BM
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (13) : 5965 - 5968
  • [9] Long-term acceptance of skin and cardiac allografts after blocking CD40 and CD28 pathways
    Larsen, CP
    Elwood, ET
    Alexander, DZ
    Ritchie, SC
    Hendrix, R
    TuckerBurden, C
    Cho, HR
    Aruffo, A
    Hollenbaugh, D
    Linsley, PS
    Winn, KJ
    Pearson, TC
    [J]. NATURE, 1996, 381 (6581) : 434 - 438
  • [10] LEE CK, 1990, MOL IMMUNOL, V27, P1137