HIP12 is a non-proapoptotic member of a gene family including HIP1, an interacting protein with huntingtin

被引:38
作者
Chopra, VS
Metzler, M
Rasper, DM
Engqvist-Goldstein, AEY
Singaraja, R
Gan, L
Fichter, KM
McCutcheon, K
Drubin, H
Nicholson, DW
Hayden, MR
机构
[1] Univ British Columbia, Dept Med Genet, Vancouver, BC V5Z 4H4, Canada
[2] Univ British Columbia, Ctr Mol Med & Therapeut, Vancouver, BC V5Z 4H4, Canada
[3] Univ Calif Berkeley, Dept Mol & Cell Biol, Berkeley, CA USA
[4] Merck Frosst Ctr Therapeut Res, Dept Biochem & Mol Biol, Montreal, PQ, Canada
关键词
D O I
10.1007/s003350010195
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
Huntingtin-interacting protein 1 (HIP1) is a membrane-associated protein that interacts with huntingtin, the protein altered in Huntington disease. HIP1 shows homology to S1a2p, a protein essential for the assembly and function of the cytoskeleton and endocytosis in Saccharomyces cerevisiae. We have determined that the HIP1 gene comprises 32 exons spanning approximately 215 kb of genomic DNA and gives rise to two alternate splice forms termed HIP1-1 and HIP1-2. Additionally, we have identified a novel protein termed HIP12 with significant sequence and biochemical similarities to HIP1 and high sequence similarity to S1a2p. HIP12 differs from HIP1 in its pattern of expression both at the mRNA and protein level. However, HIP1 and HIP12 are both found within the brain and show a similar subcellular distribution pattern. In contrast to HIP1, which is toxic in cell culture, HIP12 does not confer toxicity in the same assay systems. Interestingly, HIP12 does not interact with huntingtin but can interact with HIP 1, suggesting a potential interaction in vivo that may influence the function of each respective protein.
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页码:1006 / 1015
页数:10
相关论文
共 39 条
[1]   GCS1, an Arf guanosine triphosphatase-activating protein in Saccharomyces cerevisiae, is required for normal actin cytoskeletal organization in vivo and stimulates actin polymerization in vitro [J].
Blader, IJ ;
Cope, MJTV ;
Jackson, TR ;
Profit, AA ;
Greenwood, AF ;
Drubin, DG ;
Prestwich, GD ;
Theibert, AB .
MOLECULAR BIOLOGY OF THE CELL, 1999, 10 (03) :581-596
[2]   Fast transport and retrograde movement of huntingtin and HAP 1 in axons [J].
BlockGalarza, J ;
Chase, KO ;
Sapp, E ;
Vaughn, KT ;
Vallee, RB ;
DiFiglia, M ;
Aronin, N .
NEUROREPORT, 1997, 8 (9-10) :2247-2251
[3]   ARF PROTEINS - THE MEMBRANE TRAFFIC POLICE [J].
BOMAN, AL ;
KAHN, RA .
TRENDS IN BIOCHEMICAL SCIENCES, 1995, 20 (04) :147-150
[4]   Huntingtin-associated protein 1 (HAP1) binds to a Trio-like polypeptide, with a rad guanine nucleotide exchange factor domain [J].
Colomer, V ;
Engelender, S ;
Sharp, AH ;
Duan, K ;
Cooper, JK ;
Lanahan, A ;
Lyford, G ;
Worley, P ;
Ross, CA .
HUMAN MOLECULAR GENETICS, 1997, 6 (09) :1519-1525
[5]   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
[6]   Huntingtin-associated protein 1 (HAP1) interacts with the p150(Glued) subunit of dynactin [J].
Engelender, S ;
Sharp, AH ;
Colomer, V ;
Tokito, MK ;
Lanahan, A ;
Worley, P ;
Holzbaur, ELF ;
Ross, CA .
HUMAN MOLECULAR GENETICS, 1997, 6 (13) :2205-2212
[7]   An actin-binding protein of the Sla2/Huntingtin interacting protein 1 family is a novel component of clathrin-coated pits and vesicles [J].
Engqvist-Goldstein, ÅEY ;
Kessels, MM ;
Chopra, VS ;
Hayden, MR ;
Drubin, DG .
JOURNAL OF CELL BIOLOGY, 1999, 147 (07) :1503-1518
[8]  
GEITZ RD, 1996, CELL BIOL LAB MANUAL, pR30
[9]   Cleavage of huntingtin by apopain, a proapoptotic cysteine protease, is modulated by the polyglutamine tract [J].
Goldberg, YP ;
Nicholson, DW ;
Rasper, DM ;
Kalchman, MA ;
Koide, HB ;
Graham, RK ;
Bromm, M ;
KazemiEsfarjani, P ;
Thornberry, NA ;
Vaillancourt, JP ;
Hayden, MR .
NATURE GENETICS, 1996, 13 (04) :442-449
[10]   IDENTIFICATION AND LOCALIZATION OF HUNTINGTIN IN BRAIN AND HUMAN LYMPHOBLASTOID CELL-LINES WITH ANTI-FUSION PROTEIN ANTIBODIES [J].
GUTEKUNST, CA ;
LEVEY, AI ;
HEILMAN, CJ ;
WHALEY, WL ;
YI, H ;
NASH, NR ;
REES, HD ;
MADDEN, JJ ;
HERSCH, SM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (19) :8710-8714