Computational and biological analysis of 680 kb of DNA sequence from the human 5q31 cytokine gene cluster region

被引:114
作者
Frazer, KA [1 ]
Ueda, Y [1 ]
Zhu, YW [1 ]
Gifford, VR [1 ]
Garofalo, MR [1 ]
Mohandas, N [1 ]
Martin, CH [1 ]
Palazzolo, MJ [1 ]
Cheng, JF [1 ]
Rubin, EM [1 ]
机构
[1] UNIV CALIF BERKELEY,LAWRENCE BERKELEY LAB,CTR HUMAN GENOME,BERKELEY,CA 94720
来源
GENOME RESEARCH | 1997年 / 7卷 / 05期
关键词
D O I
10.1101/gr.7.5.495
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
With the human genome project advancing into what will be a 7- to 10-year DNA sequencing phase, we are presented with the challenge of developing strategies to convert genomic sequence data, as they become available, into biologically meaningful information. We have analyzed 680 kb of noncontiguous DNA sequence from a 1-Mb region of human chromosome 5q31, coupling computational analysis with gene expression studies of tissues isolated from humans as well as from mice containing human YAC transgenes. This genomic interval has been noted previously for containing the cytokine gene cluster and a quantitative trait locus associated with inflammatory diseases. Our analysis identified and verified expression of 16 new genes, as well as 7 previously known genes. Of the total of 23 genes in this region, 78% had similarity matches to sequences in protein databases and 83% had exact expressed sequence tag [EST] database matches. Comparative mapping studies of eight of the new human genes discovered in the 5q31 region revealed chat all are located in the syntenic region of mouse chromosome 11q. Our analysis demonstrates an approach For examining human sequence as it is made available from large sequencing programs and has resulted in the discovery of several biomedically important genes, including a cyclin, a transcription factor that is homologous to an oncogene, a protein involved in DNA repair, and several new members of a family of transporter proteins.
引用
收藏
页码:495 / 512
页数:18
相关论文
共 44 条
  • [1] ADAMS MD, 1995, NATURE, V377, P3
  • [2] KINESIN FAMILY IN MURINE CENTRAL-NERVOUS-SYSTEM
    AIZAWA, H
    SEKINE, Y
    TAKEMURA, R
    ZHANG, ZZ
    NANGAKU, M
    HIROKAWA, N
    [J]. JOURNAL OF CELL BIOLOGY, 1992, 119 (05) : 1287 - 1296
  • [3] ALTSCHUL SF, 1990, J MOL BIOL, V215, P403, DOI 10.1006/jmbi.1990.9999
  • [4] EVIDENCE FOR LINKAGE OF TOTAL SERUM IGE AND BRONCHIAL HYPERRESPONSIVENESS TO CHROMOSOME 5Q - A MAJOR REGULATORY LOCUS IMPORTANT IN ASTHMA
    BLEECKER, ER
    AMELUNG, PJ
    LEVITT, RC
    POSTMA, DS
    MEYERS, DA
    [J]. CLINICAL AND EXPERIMENTAL ALLERGY, 1995, 25 : 84 - 88
  • [5] BLEECKER ER, 1995, CLIN EXP ALLERGY S2, V25, P95
  • [6] Normalization and subtraction: Two approaches to facilitate gene discovery
    Bonaldo, MDF
    Lennon, G
    Soares, MB
    [J]. GENOME RESEARCH, 1996, 6 (09): : 791 - 806
  • [7] Complete genome sequence of the methanogenic archaeon, Methanococcus jannaschii
    Bult, CJ
    White, O
    Olsen, GJ
    Zhou, LX
    Fleischmann, RD
    Sutton, GG
    Blake, JA
    FitzGerald, LM
    Clayton, RA
    Gocayne, JD
    Kerlavage, AR
    Dougherty, BA
    Tomb, JF
    Adams, MD
    Reich, CI
    Overbeek, R
    Kirkness, EF
    Weinstock, KG
    Merrick, JM
    Glodek, A
    Scott, JL
    Geoghagen, NSM
    Weidman, JF
    Fuhrmann, JL
    Nguyen, D
    Utterback, TR
    Kelley, JM
    Peterson, JD
    Sadow, PW
    Hanna, MC
    Cotton, MD
    Roberts, KM
    Hurst, MA
    Kaine, BP
    Borodovsky, M
    Klenk, HP
    Fraser, CM
    Smith, HO
    Woese, CR
    Venter, JC
    [J]. SCIENCE, 1996, 273 (5278) : 1058 - 1073
  • [8] INFORMATION ENHANCEMENT METHODS FOR LARGE-SCALE SEQUENCE-ANALYSIS
    CLAVERIE, JM
    STATES, DJ
    [J]. COMPUTERS & CHEMISTRY, 1993, 17 (02): : 191 - 201
  • [9] Claverie JM, 1996, METHOD ENZYMOL, V266, P212
  • [10] Human/mouse homology relationships
    DeBry, RW
    Seldin, MF
    [J]. GENOMICS, 1996, 33 (03) : 337 - 351