High mobility group proteins 1 and 2 stimulate binding of a specific transcription factor to the adenovirus major late promoter
Open Access
- 25 February 1988
- journal article
- research article
- Published by Oxford University Press (OUP) in Nucleic Acids Research
- Vol. 16 (4), 1471-1486
- https://doi.org/10.1093/nar/16.4.1471
Abstract
High mobility group proteins 1 and 2 (HMGs 1 and 2) are abundant chromosomal proteins which are believed to be preferentially associated with regions of active chromatin. Our previous results have shown that RMCs 1 and 2 can significantly stimulate specific transcription in vitro from the adenovirus major late promoter. This stimulation is now shown to be due, at least in part, to the influence of HMGs 1 and 2 on binding of a specific transcription factor (MLTF) upstream of the start site of the gene to a region (−66 to −51) which is required for optimal transcription both in vivo and in vitro HMGs 1 and 2 cause both an increase in the rate of binding of the transcription factor to the DNA and alterations to the pattern of the DNaseI footprint of the factor on the DNA. Different binding states of the factor are also observed dependent on the presence of MgCl2, the factor being bound but not protecting the binding region from DNasel in the absence of NgC12.Keywords
This publication has 31 references indexed in Scilit:
- Interaction of a gene-specific transcription factor with the adenovirus major late promoter upstream of the TATA box regionCell, 1985
- Factors involved in specific transcription by human RNA polymerase II: analysis by a rapid and quantitative in vitro assay.Proceedings of the National Academy of Sciences, 1985
- Binding of the glucocorticoid receptor complex to the nucleosomal core in the P1798 mouse lymphosarcomaMolecular and Cellular Endocrinology, 1985
- Conformation and domain structure of the non‐histone chromosomal proteins HMG 1 and 2European Journal of Biochemistry, 1984
- In vitro transcription from the adenovirus 2 major late promoter utilizing templates truncated at promoter-proximal sites.Journal of Biological Chemistry, 1984
- Enrichment of transcribed and newly replicated DNA in soluble chromatin released from nuclei by mild micrococcal nuclease digestionBiochimica et Biophysica Acta (BBA) - Gene Structure and Expression, 1984
- Generation and functional analyses for base-substitution mutants of the adenovirus 2 major late promoterNucleic Acids Research, 1984
- Stimulation ofin vitrotranscription by the upstream element of the adenovirus-2 major late promoter involves a specific factorNucleic Acids Research, 1984
- Sequences upstream from the T-A-T-A box are required in vivo and in vitro for efficient transcription from the adenovirus serotype 2 major late promoter.Proceedings of the National Academy of Sciences, 1982
- Domain structure in high molecular weight high mobility group nonhistone chromatin proteinsNature, 1982