Capturing nuclear sequence-specific DNA-binding proteins by using simian virus 40-derived minichromosomes
Molecular and Cellular Biology, ISSN: 0270-7306, Vol: 8, Issue: 2, Page: 982-987
1988
- 6Citations
- 5Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
Citation Benchmarking is provided by Scopus and SciVal and is different from the metrics context provided by PlumX Metrics.
Metrics Details
- Citations6
- Citation Indexes6
- CrossRef3
- Captures5
- Readers5
Article Description
We have used recombinant simian virus 40 (SV40) minichromosomes to retrieve sequence-specific DNA-binding proteins derived from the cell nucleus of COS-7 cells. We showed that the transcription factors AP-1 and Sp1 are stably bound to the SV40 DNA late in viral infection. Under similar conditions, minichromosomes carrying the rat insulin (rINS1) enhancer, which is under negative regulation in COS-7 cells, bound two proteins which mapped to distinct regions of the rINS1 enhancer. The SV40 P element competed for one of these proteins which bound to the region from -198 to -230. This factor may be related to AP-1. The other factor selectively bound a regulatory element in the region from -92 to -124 of the insulin enhancer. These proteins may play a role in regulating the rINS1 enhancer function.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=0023832689&origin=inward; http://dx.doi.org/10.1128/mcb.8.2.982; http://dx.doi.org/10.1128/mcb.8.2.982-987.1988; http://www.ncbi.nlm.nih.gov/pubmed/2832746; http://mcb.asm.org/lookup/doi/10.1128/MCB.8.2.982; https://www.tandfonline.com/doi/full/10.1128/mcb.8.2.982-987.1988; https://syndication.highwire.org/content/doi/10.1128/MCB.8.2.982; https://dx.doi.org/10.1128/mcb.8.2.982; https://mcb.asm.org/content/8/2/982; http://mcb.asm.org/content/8/2/982; https://mcb.asm.org/content/8/2/982.abstract; https://mcb.asm.org/content/8/2/982.full.pdf; https://mcb.asm.org/content/mcb/8/2/982.full.pdf
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