Identification of a novel human cytokine gene in the interleukin gene cluster on chromosome 2q12-14

被引:122
|
作者
Bensen, JT
Dawson, PA
Mychaleckyj, JC
Bowden, DW
机构
[1] Wake Forest Univ, Bowman Gray Sch Med, Dept Biochem, Winston Salem, NC 27157 USA
[2] Wake Forest Univ, Bowman Gray Sch Med, Program Mol Med, Winston Salem, NC 27157 USA
[3] Wake Forest Univ, Bowman Gray Sch Med, Dept Internal Med, Winston Salem, NC 27157 USA
[4] Wake Forest Univ, Bowman Gray Sch Med, Dept Physiol & Pharmacol, Winston Salem, NC 27157 USA
[5] Wake Forest Univ, Bowman Gray Sch Med, Dept Publ Hlth Sci, Winston Salem, NC 27157 USA
[6] Wake Forest Univ, Bowman Gray Sch Med, Ctr Human Genom, Winston Salem, NC 27157 USA
来源
关键词
D O I
10.1089/107999001753289505
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Genes in the interleukin-1 (IL-1) gene cluster on human chromosome 2 play an important role in mediating inflammatory responses and are associated with numerous diseases. We have identified a novel IL-1-like gene, IL-1F10, on human chromosome 2q13-14.1 near the IL-1 receptor antagonist gene (IL-1RN). The IL-1F10 gene is encoded by 5 exons spanning over 7.8 kb of genomic DNA. The 1008-bp IL-1F10 cDNA encodes a 152-amino acid protein that shares between 41% and 43% amino acid identity with human IL-1 receptor antagonist (IL-1Ra) and FIL-1 delta, respectively. IL-1F10 shares characteristics of the IL-1Ra family, including key amino acid consensus sequences and a similar genomic structure. By multitissue first-strand cDNA PCR analysis, IL-1F10 mRNA is expressed in heart, placenta, fetal liver, spleen, thymus, and tonsil. The expression in a variety of immune tissues and similarity to IL-1Ra suggest a role of IL-1F10 in the inflammatory response.
引用
收藏
页码:899 / 904
页数:6
相关论文
共 50 条
  • [31] Localization of a novel gene for congenital nonsyndromic simple microphthalmia to chromosome 2q11-14
    Hui Li
    Jia-Xin Wang
    Cheng-Ye Wang
    Ping Yu
    Qiang Zhou
    Yong-Gang Chen
    Lu-Hang Zhao
    Ya-Ping Zhang
    Human Genetics, 2008, 122 : 589 - 593
  • [32] Organization and expression of the human serpin gene cluster at 14q32.1
    Marsden, MD
    Fournier, REK
    FRONTIERS IN BIOSCIENCE-LANDMARK, 2005, 10 : 1768 - 1778
  • [33] Identification and molecular characterization of TM7SF2 in the FAUNA gene cluster on human chromosome 11q13
    Lemmens, IH
    Kas, K
    Merregaert, J
    Van de Ven, WJM
    GENOMICS, 1998, 49 (03) : 437 - 442
  • [34] Localization of a novel gene for congenital nonsyndromic simple microphthalmia to chromosome 2q11-14
    Li, Hui
    Wang, Jia-Xin
    Wang, Cheng-Ye
    Yu, Ping
    Zhou, Qiang
    Chen, Yong-Gang
    Zhao, Lu-Hang
    Zhang, Ya-Ping
    HUMAN GENETICS, 2008, 122 (06) : 589 - 593
  • [35] Identification and characterization of C6orf37, a novel candidate human retinal disease gene on chromosome 6q14
    Lagali, PS
    Kakuk, LE
    Griesinger, IB
    Wong, PW
    Ayyagari, R
    BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2002, 293 (01) : 356 - 365
  • [36] Identification of a large novel imprinted gene cluster on mouse proximal chromosome 6
    Ono, R
    Shiura, H
    Aburatani, H
    Kohda, T
    Kaneko-Ishino, T
    Ishino, F
    GENOME RESEARCH, 2003, 13 (07) : 1696 - 1705
  • [37] Identification and characterization of Crumbs homolog 2 gene at human chromosome 9q33.3
    Katoh, M
    Katoh, M
    INTERNATIONAL JOURNAL OF ONCOLOGY, 2004, 24 (03) : 743 - 749
  • [38] Identification of an imprinted gene, Meg3/Gtl2 and its human homologue MEG3, first mapped on mouse distal chromosome 12 and human chromosome 14q
    Miyoshi, N
    Wagatsuma, H
    Wakana, S
    Shiroishi, T
    Nomura, M
    Aisaka, K
    Kohda, T
    Surani, MA
    Kaneko-Ishino, T
    Ishino, F
    GENES TO CELLS, 2000, 5 (03) : 211 - 220
  • [39] Linkage of the gene for the triple A syndrome to chromosome 12q13 near the type II keratin gene cluster
    Weber, A
    Wienker, TF
    Jung, M
    Easton, D
    Dean, HJ
    Heinrichs, C
    Reis, A
    Clark, AJL
    HUMAN MOLECULAR GENETICS, 1996, 5 (12) : 2061 - 2066
  • [40] The human type II keratin gene cluster on chromosome 12q13.13: Final count or hidden secrets?
    Bowden, PE
    JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2005, 124 (03) : XV - XVII