Molecular Biology of the Cell track citations

Home Help [Feedback] [For Subscribers] [Archive] [Search] [Contents]
 QUICK SEARCH:   [advanced]


     


This Article
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
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 Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Acton, S. L.
Right arrow Articles by Jackson, A. P.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Acton, S. L.
Right arrow Articles by Jackson, A. P.

Alteration of clathrin light chain expression by transfection and gene disruption

SL Acton, DH Wong, P Parham, FM Brodsky and AP Jackson

Department of Pharmacy, School of Pharmacy and Microbiology and Immunology, University of California, San Francisco 94143-0446.

The light chain subunits of clathrin, LCa and LCb, have been implicated in the regulation of coated vesicle disassembly and other aspects of clathrin cycling within the cell. The potential for functional specialization of each light chain is suggested by tissue-specific variation in the relative amounts of the two light chains and by conservation of differences between LCa and LCb sequences during evolution. To investigate whether there might be exclusive roles for LCa and LCb in clathrin function, the expression of LCa was manipulated in C1R lymphoid cells and PC12 pheochromocytoma cells by transfection with light chain cDNA. These two cell lines differ in their ratios of LCa to LCb, expressing 86 and 25% LCa, respectively. After transfection with exogenous human LCa cDNA, a PC12 cell derivative was produced that completely lost the ability to manufacture LCa. Loss of LCa expression was found to be because of gene disruption and consequent lack of mRNA transcription. In C1R cells, the normally high level of LCa expression was reduced to 25% by overexpression of transfected LCb cDNA under the control of an inducible promoter. The C1R transfectants with reduced levels of LCa and the LCa-negative PC12 transfectant grow normally and show no change in clathrin distribution, clathrin assembly level, or impairment of endocytosis or secretion compared with wild-type cells and cells transfected with vectors lacking light chain cDNA. However, subtle alterations in the hsc70-mediated clathrin uncoating process were observed for vesicles derived from the LCa-negative cells, reflecting the preferential activity of LCa in stimulating the in vitro uncoating reaction.

Volume 4, Issue 6, pp. 647-660, 06/01/1993
Copyright © 1993 by The American Society for Cell Biology




This article has been cited by other articles:


Home page
Proc. Natl. Acad. Sci. USAHome page
V. Poupon, M. Girard, V. Legendre-Guillemin, S. Thomas, L. Bourbonniere, J. Philie, N. A. Bright, and P. S. McPherson
Clathrin light chains function in mannose phosphate receptor trafficking via regulation of actin assembly
PNAS, January 8, 2008; 105(1): 168 - 173.
[Abstract] [Full Text] [PDF]


Home page
Mol. Cell. ProteomicsHome page
J. Madoz-Gurpide, M. Canamero, L. Sanchez, J. Solano, P. Alfonso, and J. I. Casal
A Proteomics Analysis of Cell Signaling Alterations in Colorectal Cancer
Mol. Cell. Proteomics, December 1, 2007; 6(12): 2150 - 2164.
[Abstract] [Full Text] [PDF]


Home page
J. Virol.Home page
A. A. Kolokoltsov, D. Deniger, E. H. Fleming, N. J. Roberts Jr., J. M. Karpilow, and R. A. Davey
Small Interfering RNA Profiling Reveals Key Role of Clathrin-Mediated Endocytosis and Early Endosome Formation for Infection by Respiratory Syncytial Virus
J. Virol., July 15, 2007; 81(14): 7786 - 7800.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
J. Xiao, R. Dai, L. Negyessy, and C. Bergson
Calcyon, a Novel Partner of Clathrin Light Chain, Stimulates Clathrin-mediated Endocytosis
J. Biol. Chem., June 2, 2006; 281(22): 15182 - 15193.
[Abstract] [Full Text] [PDF]


Home page
Mol. Biol. CellHome page
A. C. Theos, D. Tenza, J. A. Martina, I. Hurbain, A. A. Peden, E. V. Sviderskaya, A. Stewart, M. S. Robinson, D. C. Bennett, D. F. Cutler, et al.
Functions of Adaptor Protein (AP)-3 and AP-1 in Tyrosinase Sorting from Endosomes to Melanosomes
Mol. Biol. Cell, November 1, 2005; 16(11): 5356 - 5372.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
C.-Y. Chen and F. M. Brodsky
Huntingtin-interacting Protein 1 (Hip1) and Hip1-related Protein (Hip1R) Bind the Conserved Sequence of Clathrin Light Chains and Thereby Influence Clathrin Assembly in Vitro and Actin Distribution in Vivo
J. Biol. Chem., February 18, 2005; 280(7): 6109 - 6117.
[Abstract] [Full Text] [PDF]


Home page
J. Exp. Med.Home page
V. L. Crotzer, A. S. Mabardy, A. Weiss, and F. M. Brodsky
T Cell Receptor Engagement Leads to Phosphorylation of Clathrin Heavy Chain during Receptor Internalization
J. Exp. Med., April 5, 2004; 199(7): 981 - 991.
[Abstract] [Full Text] [PDF]


Home page
Proc. Natl. Acad. Sci. USAHome page
D. Yang, F. Buchholz, Z. Huang, A. Goga, C.-Y. Chen, F. M. Brodsky, and J. M. Bishop
Short RNA duplexes produced by hydrolysis with Escherichia coli RNase III mediate effective RNA interference in mammalian cells
PNAS, July 23, 2002; 99(15): 9942 - 9947.
[Abstract] [Full Text] [PDF]


Home page
Physiol. Rev.Home page
A. L. Fink
Chaperone-Mediated Protein Folding
Physiol Rev, April 1, 1999; 79(2): 425 - 449.
[Abstract] [Full Text] [PDF]


Home page
J. Cell Sci.Home page
H. Blackbourn and A. Jackson
Plant clathrin heavy chain: sequence analysis and restricted localisation in growing pollen tubes
J. Cell Sci., January 4, 1996; 109(4): 777 - 786.
[Abstract] [PDF]




Home Help [Feedback] [For Subscribers] [Archive] [Search] [Contents]