| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
Genetics, Vol. 174, 1189-1204, November 2006, Copyright © 2006
doi:10.1534/genetics.106.057604
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||





* Department of Biology, Washington University, Saint Louis, Missouri 63130,
Dipartimento di Scienze e Tecnologie Biologiche ed Ambientali, Università di Lecce, 73100 Lecce, Italy,
Cellular and Molecular Biology Program, University of Michigan, Ann Arbor, Michigan 48109,
Department of Molecular and Cell Biology, University of California, Berkeley, California 94720, ** Case School of Medicine, Case Western Reserve University, Cleveland, Ohio 44106 and 
Dipartimento di Genetica e Biologia Molecolare, Università di Roma La Sapienza, 00185 Rome, Italy
1 Corresponding author: Department of Biology, CB-1229, Washington University, 1 Brookings Dr., St. Louis, MO 63130.
E-mail: shaffer{at}biology.wustl.edu
365 kDa) and HP2-S (
175 kDa), lacking exons 5 and 6. In general, mutations that affect only the larger isoform result in more pronounced defects than do mutations common to both isoforms. This suggests that an imbalance between large and small isoforms is particularly deleterious. These results indicate a role for HP2 in the structural organization of chromosomes and in heterochromatin-induced gene silencing and show that the larger isoform plays a critical role in these processes. This article has been cited by other articles:
![]() |
K. A. Haynes, E. Gracheva, and S. C. R. Elgin A Distinct Type of Heterochromatin Within Drosophila melanogaster Chromosome 4 Genetics, March 1, 2007; 175(3): 1539 - 1542. [Abstract] [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |