TY - JOUR
T1 - Interactions between cellular regulatory proteins and a unique sequence region in the human cytomegalovirus major immediate-early promoter
AU - Ghazal, Peter
AU - Lubon, Henryk
AU - Reynolds-Kohler, Catherine
AU - Hennighausen, Lothar
AU - Nelson, Jay A.
N1 - Funding Information:
We thank B. Fleckenstein for recombinant plasmids pRR55 and pRR56/1 and P. Rosenfeld and T. Kelly for their gift of purified preparation of NFl This is Publication No. 5912-IMM from the Department of Immunology, Scripps Clinic and Research Foundation, La Jolla, California 92037. This work was supported in part by USHPS Grant AI-21 640, a Faculty Research Award from the American Cancer Society (JAN), and funds provided by the State of California and allocated on the recommendation of the Universitywide Task Force on AIDS.
PY - 1990/1
Y1 - 1990/1
N2 - Transcription from the human cytomegalovirus major immediate-early promoter is dependent on host-cell regulatory proteins. The interactions between cellular nuclear proteins and a unique sequence located from nucleotide position -660 to -540 was investigated. The unique region presents a defined target for multiple distinct DNA-binding proteins which appear, in part, to have overlapping binding sites. A minimum of five sequence-specific DNA-binding activities that interact with sequences between -632 and -602, -602 and -557, -602 and -590, -563 and -540, and -602 and -582 were detected. Evidence is presented to suggest that the -632 to -602 site, a previously characterized nuclear factor 1 binding site, does not bind NF1 but strongly interacts with a distinct cellular factor. The binding of cellular proteins to the unique sequence region was shown to be important in directing transcription from the major immediate-early promoter.
AB - Transcription from the human cytomegalovirus major immediate-early promoter is dependent on host-cell regulatory proteins. The interactions between cellular nuclear proteins and a unique sequence located from nucleotide position -660 to -540 was investigated. The unique region presents a defined target for multiple distinct DNA-binding proteins which appear, in part, to have overlapping binding sites. A minimum of five sequence-specific DNA-binding activities that interact with sequences between -632 and -602, -602 and -557, -602 and -590, -563 and -540, and -602 and -582 were detected. Evidence is presented to suggest that the -632 to -602 site, a previously characterized nuclear factor 1 binding site, does not bind NF1 but strongly interacts with a distinct cellular factor. The binding of cellular proteins to the unique sequence region was shown to be important in directing transcription from the major immediate-early promoter.
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U2 - 10.1016/0042-6822(90)90049-W
DO - 10.1016/0042-6822(90)90049-W
M3 - Article
C2 - 2152991
AN - SCOPUS:0025022515
SN - 0042-6822
VL - 174
SP - 18
EP - 25
JO - Virology
JF - Virology
IS - 1
ER -