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Identification of the DNA binding site for NGFI-B by genetic selection in yeast.

作者信息

Wilson T E, Fahrner T J, Johnston M, Milbrandt J

机构信息

Department of Pathology, Washington University School of Medicine, St. Louis, MO 63110.

出版信息

Science. 1991 May 31;252(5010):1296-300. doi: 10.1126/science.1925541.

Abstract

An in vivo selection system for isolating targets of DNA binding proteins in yeast was developed and used to identify the DNA binding site for the NGFI-B protein, a member of the steroid-thyroid hormone receptor superfamily. The feasibility of the technique was verified by selecting DNA fragments that contained binding sites for GCN4, a well-characterized yeast transcriptional activator. The DNA binding domain of NGFI-B, expressed as part of a LexA-NGFI-B-GAL4 chimeric activator, was then used to isolate a rat genomic DNA fragment that contained an NGFI-B binding site. The NGFI-B response element (NBRE) is similar to but functionally distinct from elements recognized by the estrogen and thyroid hormone receptors and the hormone receptor-like proteins COUP-TF, CF1, and H-2RIIBP. Cotransfection experiments in mammalian cells demonstrated that NGFI-B can activate transcription from the NBRE with or without its putative ligand binding domain.

摘要

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