Literature DB >> 6722875

Structure and function of the adenovirus origin of replication.

D R Rawlins, P J Rosenfeld, R J Wides, M D Challberg, T J Kelly.   

Abstract

Efficient initiation of adenovirus DNA replication requires the presence of specific terminal nucleotide sequences that collectively constitute the viral origin of replication. Using plasmids with deletions or base substitutions in a cloned segment of DNA derived from the terminus of the adenovirus 2 genome, we have demonstrated that the origin contains two functionally distinct regions. The first 18 bp of the viral genome are sufficient to support a limited degree of initiation. However, the presence of a sequence in the region between nucleotides 19 and 67 greatly enhances the efficiency of the initiation reaction. This region contains a specific binding site for a protein present in uninfected cells (KD = 2 X 10(-11) M). The bound protein protects the DNA segment between base pairs 19 and 43 from attack by DNAase I. Studies with deletion mutants indicate that binding of the cellular protein is responsible for the enhancement of initiation.

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Year:  1984        PMID: 6722875     DOI: 10.1016/0092-8674(84)90327-1

Source DB:  PubMed          Journal:  Cell        ISSN: 0092-8674            Impact factor:   41.582


  77 in total

Review 1.  Recognition mechanisms in the synthesis of animal virus DNA.

Authors:  R T Hay; W C Russell
Journal:  Biochem J       Date:  1989-02-15       Impact factor: 3.857

2.  Nuclear factor I is specifically targeted to discrete subnuclear sites in adenovirus type 2-infected cells.

Authors:  J Bosher; A Dawson; R T Hay
Journal:  J Virol       Date:  1992-05       Impact factor: 5.103

3.  Protein-DNA interaction within one cloned chloroplast DNA replication origin of Chlamydomonas.

Authors:  Z Q Nie; D Y Chang; M Wu
Journal:  Mol Gen Genet       Date:  1987-09

4.  Identification of a protein that interacts with the nuclear factor-1 (NF-1) binding site in cells that do not express NF-1: comparison to NF-1, cellular distribution, and effect on transcription.

Authors:  J J McQuillan; G D Rosen; T M Birkenmeier; D C Dean
Journal:  Nucleic Acids Res       Date:  1991-12-11       Impact factor: 16.971

5.  Identification of a signal necessary for initiation of reverse transcription of the hepadnavirus genome.

Authors:  C Seeger; J Maragos
Journal:  J Virol       Date:  1991-10       Impact factor: 5.103

6.  Analysis of multiple forms of nuclear factor I in human and murine cell lines.

Authors:  N Goyal; J Knox; R M Gronostajski
Journal:  Mol Cell Biol       Date:  1990-03       Impact factor: 4.272

Review 7.  The MRE11-RAD50-NBS1 Complex Conducts the Orchestration of Damage Signaling and Outcomes to Stress in DNA Replication and Repair.

Authors:  Aleem Syed; John A Tainer
Journal:  Annu Rev Biochem       Date:  2018-04-25       Impact factor: 23.643

8.  Dual function of a nuclear factor I binding site in MMTV transcription regulation.

Authors:  E Buetti; B Kühnel; H Diggelmann
Journal:  Nucleic Acids Res       Date:  1989-04-25       Impact factor: 16.971

9.  Physical interaction of tumour suppressor p53/p73 with CCAAT-binding transcription factor 2 (CTF2) and differential regulation of human high-mobility group 1 (HMG1) gene expression.

Authors:  Hidetaka Uramoto; Hiroto Izumi; Gunji Nagatani; Haruki Ohmori; Naofumi Nagasue; Tomoko Ise; Takeshi Yoshida; Kosei Yasumoto; Kimitoshi Kohno
Journal:  Biochem J       Date:  2003-04-15       Impact factor: 3.857

10.  Analysis of nuclear factor I binding to DNA using degenerate oligonucleotides.

Authors:  R M Gronostajski
Journal:  Nucleic Acids Res       Date:  1986-11-25       Impact factor: 16.971

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