A mouse TRAPP-related protein is involved in pigmentation

被引:24
作者
Gwynn, Babette [1 ]
Smith, Richard S. [1 ]
Rowe, Lucy B. [1 ]
Taylor, Benjamin A. [1 ]
Peters, Luanne L. [1 ]
机构
[1] Jackson Lab, Bar Harbor, ME 04609 USA
关键词
melanosomes; pigmentation; retinal pigmented epithelium; mouse mutation;
D O I
10.1016/j.ygeno.2006.04.002
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
We identified a new spontaneous recessive mutation in the mouse, mhyp (mosaic hypopigmentation), in a screen for novel proviral integration sites in a multiple ecotropic provirus mapping stock. Integration of an 8.4-kb retrovirus results in mosaic loss of coat pigment in mhyp homozygotes. Patchy loss of pigmentation in the retinal pigmented epithelial layer of the eye with abnormal melanosomes is also evident. We mapped mhyp to mouse chromosome 7 and cloned the underlying gene. mhyp is a defect in the Trappc6a gene. Expression of Trappc6a is markedly diminished in mhyp homozygotes. The normal protein, TRAPPC6A, is a subunit of the TRAPP (transport protein particle) I and 11 complexes. While TRAPP complexes are essential for ER-to-Golgi and intra-Golgi vesicle trafficking in yeast, TRAPP subunits participate in additional, including post-Golgi, transport events in mammals. The data implicate mammalian TRAPPC6A in vesicle trafficking during melanosome biogenesis. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:196 / 203
页数:8
相关论文
共 33 条
[1]  
ALGATE PA, 1993, ONCOGENE, V8, P1221
[2]   TRAPP stably associates with the Golgi and is required for vesicle docking [J].
Barrowman, J ;
Sacher, M ;
Ferro-Novick, S .
EMBO JOURNAL, 2000, 19 (05) :862-869
[3]   Mutants in trs120 disrupt traffic from the early endosome to the late Golgi [J].
Cai, HQ ;
Zhang, YY ;
Pypaert, M ;
Walker, L ;
Ferro-Novick, S .
JOURNAL OF CELL BIOLOGY, 2005, 171 (05) :823-833
[4]   Synbindin, a novel syndecan-2-binding protein in neuronal dendritic spines [J].
Ethell, IM ;
Hagihara, K ;
Miura, Y ;
Irie, F ;
Yamaguchi, Y .
JOURNAL OF CELL BIOLOGY, 2000, 151 (01) :53-67
[5]   The mouse pale ear (ep) mutation is the homologue of human Hermansky-Pudlak syndrome [J].
Gardner, JM ;
Wildenberg, SC ;
Keiper, NM ;
Novak, EK ;
Rusiniak, ME ;
Swank, RT ;
Puri, N ;
Finger, JN ;
Hagiwara, N ;
Lehman, AL ;
Gales, TL ;
Bayer, ME ;
King, RA ;
Brilliant, MH .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (17) :9238-9243
[6]   Functional organization of the yeast proteome by systematic analysis of protein complexes [J].
Gavin, AC ;
Bösche, M ;
Krause, R ;
Grandi, P ;
Marzioch, M ;
Bauer, A ;
Schultz, J ;
Rick, JM ;
Michon, AM ;
Cruciat, CM ;
Remor, M ;
Höfert, C ;
Schelder, M ;
Brajenovic, M ;
Ruffner, H ;
Merino, A ;
Klein, K ;
Hudak, M ;
Dickson, D ;
Rudi, T ;
Gnau, V ;
Bauch, A ;
Bastuck, S ;
Huhse, B ;
Leutwein, C ;
Heurtier, MA ;
Copley, RR ;
Edelmann, A ;
Querfurth, E ;
Rybin, V ;
Drewes, G ;
Raida, M ;
Bouwmeester, T ;
Bork, P ;
Seraphin, B ;
Kuster, B ;
Neubauer, G ;
Superti-Furga, G .
NATURE, 2002, 415 (6868) :141-147
[7]   Reduced pigmentation (rp), a mouse model of Hermansky-Pudlak syndrome, encodes a novel component of the BLOG-1 complex [J].
Gwynn, B ;
Martina, JA ;
Bonifacino, JS ;
Sviderskaya, EV ;
Lamoreux, ML ;
Bennett, DC ;
Moriyama, K ;
Huizing, M ;
Helip-Wooley, A ;
Gahl, WA ;
Webb, LS ;
Lambert, AJ ;
Peters, LL .
BLOOD, 2004, 104 (10) :3181-3189
[8]   Intracisternal A-particle element transposition into the murine β-glucuronidase gene correlates with loss of enzyme activity:: a new model for β-glucuronidase deficiency in the C3H mouse [J].
Gwynn, B ;
Lueders, K ;
Sands, MS ;
Birkenmeier, EH .
MOLECULAR AND CELLULAR BIOLOGY, 1998, 18 (11) :6474-6481
[9]   NUCLEOTIDE-SEQUENCE OF AKV MURINE LEUKEMIA-VIRUS [J].
HERR, W .
JOURNAL OF VIROLOGY, 1984, 49 (02) :471-478
[10]   Crystal structure of SEDL and its implications for a genetic disease spondyloepiphyseal dysplasia tarda [J].
Jang, SB ;
Kim, YG ;
Cho, YS ;
Suh, PG ;
Kim, KH ;
Oh, BH .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (51) :49863-49869