Complete set of eleven region-specific microdissection libraries for human chromosome 2

被引:2
作者
Kao, FT [1 ]
Tong, SH [1 ]
Whittier, A [1 ]
Yu, JW [1 ]
机构
[1] UNIV COLORADO, HLTH SCI CTR, DEPT BIOCHEM BIOPHYS & GENET, DENVER, CO 80262 USA
关键词
D O I
10.1007/BF02374376
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
The construction and characterization of II region-specific libraries for the entire human chromosome 2 have been completed including four libraries for the short arm and six libraries for the long arm, plus a library for the centromere region. These libraries were constructed using the chromosome microdissection and microcloning technology. Eight libraries have been described previously. This paper presents the final three libraries: 2q21-q22 (designated 2Q5 library), 2q11-q14 (2Q6). and 2p11.1-q11.1 (2CEN). The sizes of the dissected regions ranged between 20 and 30 Mb, with the centromere region of about 4 Mb. All these libraries are large, potentially comprising hundreds of thousands of recombinant microclones. Between 77% and 97% of the microclones were shown to derive from respective dissected regions. From 26 to 66 unique sequence microclones were isolated and characterized in detail for each library. The microclones have short inserts, ranging between 50 and 600 bp, with a mean of about 200 bp. The short inserts can be conveniently sequenced as STSs to provide high density probes for the dissected region. A plasmid sub-library containing at least 20,000 microclones, and usually more, has been prepared from each library and deposited to ATCC for general distribution. The libraries have been used effectively in constructing high resolution physical maps and for contig assembly, as well as in positional cloning of disease genes assigned to the dissected region. Comparing to other chromosomes with detailed mapping information and densely populated probes, chromosome 2 remains largely under-exploited, The availability of a complete set of region-specific libraries and unique sequence microclones from the libraries should provide valuable resources for genome analysis, high resolution physical mapping, region-specific cDNA isolation, and positional cloning for chromosome 2.
引用
收藏
页码:57 / 66
页数:10
相关论文
共 27 条
  • [1] MOLECULAR-CLONING OF APRF, A NOVEL IFN-STIMULATED GENE FACTOR-3 P91-RELATED TRANSCRIPTION FACTOR INVOLVED IN THE GP130-MEDIATED SIGNALING PATHWAY
    AKIRA, S
    NISHIO, Y
    INOUE, M
    WANG, XJ
    WEI, S
    MATSUSAKA, T
    YOSHIDA, K
    SUDO, T
    NARUTO, M
    KISHIMOTO, T
    [J]. CELL, 1994, 77 (01) : 63 - 71
  • [2] A GENE FOR AUTOSOMAL RECESSIVE LIMB-GIRDLE MUSCULAR-DYSTROPHY MAPS TO CHROMOSOME 2P
    BASHIR, R
    STRACHAN, T
    KEERS, S
    STEPHENSON, A
    MAHJNEH, I
    MARCONI, G
    NASHEF, L
    BUSHBY, KMD
    [J]. HUMAN MOLECULAR GENETICS, 1994, 3 (03) : 455 - 457
  • [3] CHOI JY, 1995, AM J HUM GENET, V57, P1081
  • [4] LINKAGE DISEQUILIBRIUM MAPPING OF A TYPE-1 DIABETES SUSCEPTIBILITY GENE (IDDM7) TO CHROMOSOME 2Q31-Q33
    COPEMAN, JB
    CUCCA, F
    HEARNE, CM
    CORNALL, RJ
    REED, PW
    RONNINGEN, KS
    UNDLIEN, DE
    NISTICO, L
    BUZZETTI, R
    TOSI, R
    POCIOT, F
    NERUP, J
    CORNELIS, F
    BARNETT, AH
    BAIN, SC
    TODD, JA
    [J]. NATURE GENETICS, 1995, 9 (01) : 80 - 85
  • [5] LINKAGE OF RECESSIVE FAMILIAL AMYOTROPHIC-LATERAL-SCLEROSIS TO CHROMOSOME 2Q33-Q35
    HENTATI, A
    BEJAOUI, K
    PERICAKVANCE, MA
    HENTATI, F
    SPEER, MC
    HUNG, WY
    FIGLEWICZ, DA
    HAINES, J
    RIMMLER, J
    BENHAMIDA, C
    BENHAMIDA, M
    BROWN, RH
    SIDDIQUE, T
    [J]. NATURE GENETICS, 1994, 7 (03) : 425 - 428
  • [6] LINKAGE OF A LOCUS FOR AUTOSOMAL-DOMINANT FAMILIAL SPASTIC PARAPLEGIA TO CHROMOSOME 2P MARKERS
    HENTATI, A
    PERICAKVANCE, MA
    LENNON, F
    WASSERMAN, B
    HENTATI, F
    JUNEJA, T
    ANGRIST, MH
    HUNG, WY
    BOUSTANY, RM
    BOHLEGA, S
    IQBAL, Z
    HUETHER, CH
    BENHAMIDA, M
    SIDDIQUE, T
    [J]. HUMAN MOLECULAR GENETICS, 1994, 3 (10) : 1867 - 1871
  • [7] REFINED GENETIC-MAPPING OF A GENE FOR FAMILIAL JUVENILE NEPHRONOPHTHISIS (NPH1) AND PHYSICAL MAPPING OF LINKED MARKERS
    HILDEBRANDT, F
    SINGHSAWHNEY, I
    SCHNIEDERS, B
    PAPENFUSS, T
    BRANDIS, M
    [J]. GENOMICS, 1995, 25 (02) : 360 - 364
  • [8] A REGION-SPECIFIC MICRODISSECTION LIBRARY FOR HUMAN-CHROMOSOME 2P23-]P21 AND THE ANALYSIS OF AN INTERSTITIAL DELETION OF 2P21
    KAO, FT
    YU, J
    QI, J
    TONG, S
    MUENKE, M
    [J]. CYTOGENETICS AND CELL GENETICS, 1995, 68 (1-2): : 17 - 18
  • [9] ISOLATION AND REFINED REGIONAL MAPPING OF EXPRESSED SEQUENCES FROM HUMAN-CHROMOSOME-21
    KAO, FT
    YU, JW
    TONG, SH
    QI, JX
    PATANJALI, SR
    WEISSMAN, SM
    PATTERSON, D
    [J]. GENOMICS, 1994, 23 (03) : 700 - 703
  • [10] CHROMOSOME MICRODISSECTION AND CLONING IN HUMAN GENOME AND GENETIC-DISEASE ANALYSIS
    KAO, FT
    YU, JW
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (05) : 1844 - 1848