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. 1989 Dec 11;17(23):9909-32.
doi: 10.1093/nar/17.23.9909.

Cis-acting sequences from mouse rDNA promote plasmid DNA amplification and persistence in mouse cells: implication of HMG-I in their function

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Free PMC article

Cis-acting sequences from mouse rDNA promote plasmid DNA amplification and persistence in mouse cells: implication of HMG-I in their function

M Wegner et al. Nucleic Acids Res. .
Free PMC article

Abstract

Searching for amplification promoting sequences within the murine rDNA cistrons, we isolated two elements from the nontranscribed spacer region. These 370 bp and 423 bp long cis-acting elements, referred to as muNTS1 and muNTS2, are localized 4.1 kb and 4.6 kb upstream the RNA polymerase I transcriptional start site. They contain ca. 50 bp long AT-rich sequences that strongly interact with a protein from nuclear extracts. The protein could be purified and identified as HMG-I. A synthetic oligonucleotide encompassing the AT-rich stretch from muNTS1 is able to substitute for the muNTS elements. A similar sequence from the nontranscribed spacer of rat has previously been reported to be important for the function of the RNA polymerase I enhancer (1). Therefore the interaction of HMG I with the muNTS elements may play a role both in the stimulation of DNA amplification and transcription.

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References

    1. Eur J Biochem. 1985 May 15;149(1):47-51 - PubMed
    1. Nucleic Acids Res. 1989 Mar 11;17(5):1867-79 - PubMed
    1. Cell. 1986 Jan 31;44(2):273-82 - PubMed
    1. Proc Natl Acad Sci U S A. 1986 Mar;83(5):1276-80 - PubMed
    1. Cell. 1986 Aug 15;46(4):521-30 - PubMed

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