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PMID: 9096322 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

In vitro evolution of terminal protein-containing genomes.

Esteban JA, Blanco L, Villar L, Salas M

Abstract

A new self-sustained terminal protein-primed DNA amplification system has been used to describe in vitro evolutionary changes affecting maintenance of the genome size of bacteriophage phi29. These changes involve generation and efficient amplification of short palindromic molecules containing an inverted duplication of one of the original DNA ends. A template-switching mechanism is proposed to account for the appearance of these molecules. After their formation, they would replicate by means of hairpin intermediates. Relevant kinetic information about this DNA replication system has been obtained from the competition between the input full-length phi29 DNA and its derived truncated versions. The physiological relevance of these molecules and the mechanisms to control their formation are discussed.

MeSH Terms
Bacillus Phages/genetics DNA, Viral/chemistry,genetics Genome, Viral Nucleic Acid Conformation Viral Proteins/genetics
Chemicals
DNA, Viral Viral Proteins
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Esteban J A
Centro de Biología Molecular Severo Ochoa, Universidad Autónoma, Canto Blanco, Madrid, Spain.
Blanco L
Villar L
Salas M
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32 references, click to expand
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Article Info
Journal
Proceedings of the National Academy of Sciences of the United States of America
Abbr.
Proc Natl Acad Sci U S A
ISSN
0027-8424
Published
1997-04-01
Pages
2921-6
Language
English
Region
United States
NLM ID
7505876
PMCID
PMC20298
Subset
IM
Grants
NIGMS NIH HHS · R01 GM027242 · United States
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