genetic locus targeted to the nuclear periphery in living cells maintains its transcriptional competence
The peripheral nuclear lamina, which is largely but not entirely associated with inactive chromatin, is considered to be an important determinant of nuclear structure and gene expression. We present here an inducible system to target a genetic locus to the nuclear lamina in living mammalian cells. U...
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Published in: | The Journal of cell biology Vol. 180; no. 1; pp. 51 - 65 |
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Main Authors: | , |
Format: | Journal Article |
Language: | English |
Published: |
United States
The Rockefeller University Press
14-01-2008
Rockefeller University Press |
Subjects: | |
Online Access: | Get full text |
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Summary: | The peripheral nuclear lamina, which is largely but not entirely associated with inactive chromatin, is considered to be an important determinant of nuclear structure and gene expression. We present here an inducible system to target a genetic locus to the nuclear lamina in living mammalian cells. Using three-dimensional time-lapse microscopy, we determined that targeting of the locus requires passage through mitosis. Once targeted, the locus remains anchored to the nuclear periphery in interphase as well as in daughter cells after passage through a subsequent mitosis. Upon transcriptional induction, components of the gene expression machinery are recruited to the targeted locus, and we visualized nascent transcripts at the nuclear periphery. The kinetics of transcriptional induction at the nuclear lamina is similar to that observed at an internal nuclear region. This new cell system provides a powerful approach to study the dynamics of gene function at the nuclear periphery in living cells. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Abbreviations used in this paper: CuO, cumate operator; LAP, lamina-associated polypeptide; pCMV, cytomegalovirus promoter; TRE, tetracycline response element. Correspondence to David L. Spector: spector@cshl.edu |
ISSN: | 0021-9525 1540-8140 |
DOI: | 10.1083/jcb.200706060 |