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Genome‐wide selection for increased copy number in Acinetobacter baylyi ADP1: locus and context‐dependent variation in gene amplification
Author(s) -
Seaton Sarah C.,
Elliott Kathryn T.,
Cuff Laura E.,
Laniohan Nicole S.,
Patel Poonam R.,
Neidle Ellen L.
Publication year - 2012
Publication title -
molecular microbiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.857
H-Index - 247
eISSN - 1365-2958
pISSN - 0950-382X
DOI - 10.1111/j.1365-2958.2011.07945.x
Subject(s) - amplicon , biology , gene duplication , locus (genetics) , genetics , copy number variation , gene , genome , gene dosage , mutant , polymerase chain reaction , gene expression
Summary Renewed interest in gene amplification stems from its importance in evolution and a variety of medical problems ranging from drug resistance to cancer. However, amplified DNA segments (amplicons) are not fully characterized in any organism. Here we report a novel Acinetobacter baylyi system for genome‐wide studies. Amplification mutants that consume aromatic compounds were selected under conditions requiring high‐level expression from three promoters in a linked set of chromosomal genes. Tools were developed to relocate these catabolic genes to any non‐essential chromosomal position, and 49 amplification mutants from five genomic contexts were characterized. Amplicon size (18–271 kb) and copy number (2–105) indicated that 30% of mutants carried more than 1 Mb of amplified DNA. Amplification features depended on genomic position. For example, amplicons from one locus were similarly sized but displayed variable copy number, whereas those from another locus were differently sized but had comparable copy number. Additionally, the importance of sequence context was highlighted in one region where amplicons differed depending on the presence of a promoter mutation in the strain from which they were selected. DNA sequences at amplicon boundaries in 19 mutants reflected illegitimate recombination. Furthermore, steady‐state duplication frequencies measured under non‐selective conditions (10 −4 to 10 −5 ) confirmed that spontaneous gene duplication is a major source of genetic variation.