5 NOVEL GENES FROM THE CRI-DU-CHAT CRITICAL REGION ISOLATED BY DIRECT SELECTION

被引:48
作者
SIMMONS, AD
GOODART, SA
GALLARDO, TD
OVERHAUSER, J
LOVETT, M
机构
[1] UNIV TEXAS, SW MED CTR, DEPT BIOCHEM, DALLAS, TX 75235 USA
[2] UNIV TEXAS, SW MED CTR, MCDERMOTT CTR, DALLAS, TX 75235 USA
[3] THOMAS JEFFERSON UNIV, DEPT BIOCHEM & MOLEC BIOL, PHILADELPHIA, PA 19107 USA
关键词
D O I
10.1093/hmg/4.2.295
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
Cri-du-chat is a well described partial aneusomy resulting from deletion of the short arm of chromosome 5. The hallmark clinical feature of cri-du-chat, a high-pitched monochromatic cry, has recently been localized to 5p15.3, separate from the remaining clinical features of the syndrome, which have been localized to 5p15.2. Five chromosome and specific probes from the latter region, designated the cri-du-chat critical region (CDCCR), were used to isolate 30 cosmids from the LANL chromosome 5 specific cosmid library. The 30 framework cosmids were used in a direct selection with three cDNA sources to isolate an initial set of expressed sequences. Nine unique cDNAs were found that hybridized to four discrete sets of cosmids in the CDCCR. The nine cDNAs are novel by sequence database comparisons, and conservatively represent four transcription units. More recently, we have also constructed a YAC contig of the CDCCR which spans approximately 2 Mb. As expected, ESTs derived from the nine novel cDNAs map back to the contig. Limited expression profiles of these cDNAs have been obtained. Two cDNAs that map to one discrete set of cosmids have different expression patterns, suggesting that they represent two different genes and increasing the number of putative genes to five. Further characterization of these genes and the estimated 100 additional genes deleted in cri-du-chat should lead to better diagnostic markers and an understanding of the molecular mechanisms of the disease.
引用
收藏
页码:295 / 302
页数:8
相关论文
共 32 条
  • [1] BASIC LOCAL ALIGNMENT SEARCH TOOL
    ALTSCHUL, SF
    GISH, W
    MILLER, W
    MYERS, EW
    LIPMAN, DJ
    [J]. JOURNAL OF MOLECULAR BIOLOGY, 1990, 215 (03) : 403 - 410
  • [2] MOLECULAR APPROACH TO ANALYZING THE HUMAN 5P DELETION SYNDROME, CRI-DU-CHAT
    CARLOCK, LR
    WASMUTH, JJ
    [J]. SOMATIC CELL AND MOLECULAR GENETICS, 1985, 11 (03) : 267 - 276
  • [3] THE OCCURRENCE OF FAMILIES OF REPETITIVE SEQUENCES IN A LIBRARY OF CLONED CDNA FROM HUMAN-LYMPHOCYTES
    CRAMPTON, JM
    DAVIES, KE
    KNAPP, TF
    [J]. NUCLEIC ACIDS RESEARCH, 1981, 9 (15) : 3821 - 3834
  • [4] FEINBERG AP, 1984, ANAL BIOCHEM, V137, P226
  • [5] HOW MANY GENES IN THE HUMAN GENOME
    FIELDS, C
    ADAMS, MD
    WHITE, O
    VENTER, JC
    [J]. NATURE GENETICS, 1994, 7 (03) : 345 - 346
  • [6] SIGNIFICANCE OF RARE MESSENGER-RNA SEQUENCES IN LIVER
    GALAU, GA
    KLEIN, WH
    BRITTEN, RJ
    DAVIDSON, EH
    [J]. ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1977, 179 (02) : 584 - 599
  • [7] A YEAST ARTIFICIAL CHROMOSOME CONTIG OF THE CRITICAL REGION FOR CRI-DU-CHAT SYNDROME
    GOODART, SA
    SIMMONS, AD
    GRADY, D
    ROJAS, K
    MOYZIS, RK
    LOVETT, M
    OVERHAUSER, J
    [J]. GENOMICS, 1994, 24 (01) : 63 - 68
  • [8] HEINKOFF S, 1991, NUCLEIC ACIDS RES, V19, P6565
  • [9] STRUCTURE AND EXPRESSION OF CDNA FOR CALPHOBINDIN-II, A HUMAN PLACENTAL COAGULATION INHIBITOR
    IWASAKI, A
    SUDA, M
    WATANABE, M
    NAKAO, H
    HATTORI, Y
    NAGOYA, T
    SAINO, Y
    SHIDARA, Y
    MAKI, M
    [J]. JOURNAL OF BIOCHEMISTRY, 1989, 106 (01) : 43 - 49
  • [10] SOMATIC-CELL HYBRID DELETION MAP OF HUMAN CHROMOSOME-18
    KLINE, AD
    ROJAS, K
    MEWAR, R
    MOSHINSKY, D
    OVERHAUSER, J
    [J]. GENOMICS, 1992, 13 (01) : 1 - 6