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Scaffold attachment regions increase reporter gene expression in stably transformed plant cells.
Author(s) -
George C. Allen,
G. Emlen Hall,
Lisa C. Childs,
A. K. Weissinger,
Steven Spiker,
William F. Thompson
Publication year - 1993
Publication title -
the plant cell
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.324
H-Index - 341
eISSN - 1532-298X
pISSN - 1040-4651
DOI - 10.1105/tpc.5.6.603
Subject(s) - biology , reporter gene , gene expression , gene , cell culture , microbiology and biotechnology , chimeric gene , position effect , transfection , regulation of gene expression , scaffold/matrix attachment region , in vitro , plant cell , genetics , chromatin remodeling
The yeast ARS-1 element contains a scaffold attachment region (SAR) that we have previously shown can bind to plant nuclear scaffolds in vitro. To test effects on expression, constructs in which a chimeric beta-glucuronidase (GUS) gene was flanked by this element were delivered into tobacco suspension cells by microprojectile bombardment. In stably transformed cell lines, GUS activity averaged 12-fold higher (24-fold on a gene copy basis) for a construct containing two flanking SARs than for a control construct lacking SARs. Expression levels were not proportional to gene copy number, as would have been predicted if the element simply reduced position effect variation. Instead, the element appeared to reduce an inhibitory effect on expression in certain transformants containing multiple gene copies. The effect on expression appears to require chromosomal integration, because SAR constructs were only twofold more active than the controls in transient assays.

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