Skip Navigation

This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrowRequest Permissions
Google Scholar
Right arrow Articles by Meisler, M. H.
Right arrow Articles by Strahler, J.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Meisler, M. H.
Right arrow Articles by Strahler, J.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

The Journal of Heredity 1984:75(2):103-106
© 1984 The American Genetic Association 75:103-106


research-article

Pigmentation and lysosomal phenotypes in mice doubly homozygous for both light-ear and pale-ear mutant alleles

Miriam H. Meisler, Leslie Wanner, and John Strahler

Department of Human Genctics, University of Michigan Ann Arbor, MI 48109

Abstract

We have developed a new strain of mice homozygous for mutant alleles at both the light-ear locus on chromosome 5 and the pale-ear locus on chromosome 19. The pigmentation pattern of the double mutants, designated light-pale, is indistinguishable from the parental type. Elevated concentrations of lysosomal enzymes observed in certain tissues of the light-ear and pale-ear singly homozygous mice also are present in the double mutants, and are quantitatively indistinguishable from either parent. Although both mutations have pleiotropic effects on organelles in several tissues, neither locus influences the secretion of pancreatic zymogen granules. The close similarity in phenotypes of light ear, pale ear, and light-pale mice suggest that the le and ep loci encode different subunits of a multlmeric protein, and that mutations affecting either subunit result in comparable losses of function.


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
Mol. Biol. CellHome page
S. M. Di Pietro, J. M. Falcon-Perez, D. Tenza, S. R.G. Setty, M. S. Marks, G. Raposo, and E. C. Dell'Angelica
BLOC-1 Interacts with BLOC-2 and the AP-3 Complex to Facilitate Protein Trafficking on Endosomes
Mol. Biol. Cell, September 1, 2006; 17(9): 4027 - 4038.
[Abstract] [Full Text] [PDF]


Home page
BloodHome page
B. Gwynn, J. A. Martina, J. S. Bonifacino, E. V. Sviderskaya, M. L. Lamoreux, D. C. Bennett, K. Moriyama, M. Huizing, A. Helip-Wooley, W. A. Gahl, et al.
Reduced pigmentation (rp), a mouse model of Hermansky-Pudlak syndrome, encodes a novel component of the BLOC-1 complex
Blood, November 15, 2004; 104(10): 3181 - 3189.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
R. Gautam, S. Chintala, W. Li, Q. Zhang, J. Tan, E. K. Novak, S. M. Di Pietro, E. C. Dell'Angelica, and R. T. Swank
The Hermansky-Pudlak Syndrome 3 (Cocoa) Protein Is a Component of the Biogenesis of Lysosome-related Organelles Complex-2 (BLOC-2)
J. Biol. Chem., March 26, 2004; 279(13): 12935 - 12942.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
J. A. Martina, K. Moriyama, and J. S. Bonifacino
BLOC-3, a Protein Complex Containing the Hermansky-Pudlak Syndrome Gene Products HPS1 and HPS4
J. Biol. Chem., August 1, 2003; 278(31): 29376 - 29384.
[Abstract] [Full Text] [PDF]


Home page
Proc. Natl. Acad. Sci. USAHome page
R. Nazarian, J. M. Falcon-Perez, and E. C. Dell'Angelica
Biogenesis of lysosome-related organelles complex 3 (BLOC-3): A complex containing the Hermansky-Pudlak syndrome (HPS) proteins HPS1 and HPS4
PNAS, July 22, 2003; 100(15): 8770 - 8775.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
P.-W. Chiang, N. Oiso, R. Gautam, T. Suzuki, R. T. Swank, and R. A. Spritz
The Hermansky-Pudlak Syndrome 1 (HPS1) and HPS4 Proteins Are Components of Two Complexes, BLOC-3 and BLOC-4, Involved in the Biogenesis of Lysosome-related Organelles
J. Biol. Chem., May 23, 2003; 278(22): 20332 - 20337.
[Abstract] [Full Text] [PDF]


Home page
BloodHome page
L. Feng, E. K. Novak, L. M. Hartnell, J. S. Bonifacino, L. M. Collinson, and R. T. Swank
The Hermansky-Pudlak syndrome 1 (HPS1) and HPS2 genes independently contribute to the production and function of platelet dense granules, melanosomes, and lysosomes
Blood, March 1, 2002; 99(5): 1651 - 1658.
[Abstract] [Full Text] [PDF]



Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.