A putative Drosophila homolog of the Huntington's disease gene

被引:49
作者
Li, Z [1 ]
Karlovich, CA
Fish, MP
Scott, MP
Myers, RM
机构
[1] Stanford Univ, Dept Genet, Sch Med, Stanford, CA 94305 USA
[2] Stanford Univ, Dept Dev Biol, Sch Med, Stanford, CA 94305 USA
[3] Stanford Univ, Howard Hughes Med Inst, Sch Med, Stanford, CA 94305 USA
关键词
D O I
10.1093/hmg/8.9.1807
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 Huntington's disease (HD) gene encodes a protein, huntingtin, with no known function and no detectable sequence similarity to other proteins in current databases. To gain insight into the normal biological role of huntingtin, we isolated and sequenced a cDNA encoding a protein that is a likely homolog of the HD gene product in Drosophila melanogaster, We also determined the complete sequence of 43 125 contiguous base pairs of genomic DNA that encompass the Drosophila HD gene, allowing the intron-exon structure and 5'- and 3'-flanking regions to be delineated, The predicted Drosophila huntingtin protein has 3583 amino acids, which is several hundred amino acids larger than any other previously characterized member of the HD family. Analysis of the genomic and cDNA sequences indicates that Drosophila HD has 29 exons, compared with the 67 exons present in vertebrate HD genes, and that Drosophila huntingtin lacks the polyglutamine and polyproline stretches present in its mammalian counterparts. The Drosophila HD mRNA is expressed in a broad range of developmental stages and in the adult, a temporal pattern of expression similar to that observed for mammalian HD transcripts. We can discern five regions of high similarity from multiple sequence alignments between Drosophila and vertebrate huntingtins, These regions may define functionally important domains within the protein.
引用
收藏
页码:1807 / 1815
页数:9
相关论文
共 45 条
[1]   GENETICS AND MOLECULAR-BIOLOGY OF HUNTINGTONS-DISEASE [J].
ALBIN, RL ;
TAGLE, DA .
TRENDS IN NEUROSCIENCES, 1995, 18 (01) :11-14
[2]  
[Anonymous], HDB SCIENCE
[3]   MOUSE HUNTINGTONS-DISEASE GENE HOMOLOG (HDH) [J].
BARNES, GT ;
DUYAO, MP ;
AMBROSE, CM ;
MCNEIL, S ;
PERSICHETTI, F ;
SRINIDHI, J ;
GUSELLA, JF ;
MACDONALD, ME .
SOMATIC CELL AND MOLECULAR GENETICS, 1994, 20 (02) :87-97
[4]   COMPARATIVE SEQUENCE-ANALYSIS OF THE HUMAN AND PUFFERFISH HUNTINGTONS-DISEASE GENES [J].
BAXENDALE, S ;
ABDULLA, S ;
ELGAR, G ;
BUCK, D ;
BERKS, M ;
MICKLEM, G ;
DURBIN, R ;
BATES, G ;
BRENNER, S ;
BECK, S ;
LEHRACH, H .
NATURE GENETICS, 1995, 10 (01) :67-76
[5]   NEUROCHEMISTRY AND TOXIN MODELS IN HUNTINGTONS-DISEASE [J].
BEAL, MF .
CURRENT OPINION IN NEUROLOGY, 1994, 7 (06) :542-547
[6]   Intranuclear neuronal inclusions in Huntington's disease and dentatorubral and pallidoluysian atrophy: Correlation between the density of inclusions and IT15 CAG triplet repeat length [J].
Becher, MW ;
Kotzuk, JA ;
Sharp, AH ;
Davies, SW ;
Bates, GP ;
Price, DL ;
Ross, CA .
NEUROBIOLOGY OF DISEASE, 1998, 4 (06) :387-397
[7]   Huntington and DRPLA proteins selectively interact with the enzyme GAPDH [J].
Burke, JR ;
Enghild, JJ ;
Martin, ME ;
Jou, YS ;
Myers, RM ;
Roses, AD ;
Vance, JM ;
Strittmatter, WJ .
NATURE MEDICINE, 1996, 2 (03) :347-350
[8]   Formation of neuronal intranuclear inclusions underlies the neurological dysfunction in mice transgenic for the HD mutation [J].
Davies, SW ;
Turmaine, M ;
Cozens, BA ;
DiFiglia, M ;
Sharp, AH ;
Ross, CA ;
Scherzinger, E ;
Wanker, EE ;
Mangiarini, L ;
Bates, GP .
CELL, 1997, 90 (03) :537-548
[9]   Aggregation of huntingtin in neuronal intranuclear inclusions and dystrophic neurites in brain [J].
DiFiglia, M ;
Sapp, E ;
Chase, KO ;
Davies, SW ;
Bates, GP ;
Vonsattel, JP ;
Aronin, N .
SCIENCE, 1997, 277 (5334) :1990-1993
[10]   HUNTINGTIN IS A CYTOPLASMIC PROTEIN ASSOCIATED WITH VESICLES IN HUMAN AND RAT-BRAIN NEURONS [J].
DIFIGLIA, M ;
SAPP, E ;
CHASE, K ;
SCHWARZ, C ;
MELONI, A ;
YOUNG, C ;
MARTIN, E ;
VONSATTEL, JP ;
CARRAWAY, R ;
REEVES, SA ;
BOYCE, FM ;
ARONIN, N .
NEURON, 1995, 14 (05) :1075-1081