Intrachromosomal recombination between direct repeats in Penicillium chrysogenum: gene conversion and deletion events

Citation
J. Casqueiro et al., Intrachromosomal recombination between direct repeats in Penicillium chrysogenum: gene conversion and deletion events, MOL G GENET, 261(6), 1999, pp. 994-1000
Citations number
38
Categorie Soggetti
Molecular Biology & Genetics
Journal title
MOLECULAR AND GENERAL GENETICS
ISSN journal
00268925 → ACNP
Volume
261
Issue
6
Year of publication
1999
Pages
994 - 1000
Database
ISI
SICI code
0026-8925(199907)261:6<994:IRBDRI>2.0.ZU;2-L
Abstract
Recombination between direct repeats has been studied in Penicillium chryso genum using strain TD7-88 (lys(-) pyr(+)), which contains two inactive copi es of the lys2 gene separated by 4.5 kb of DNA (including the pyrG gene) in its genome. Gene conversion leading to products with the lys(+) pyr(+) phe notype was observed at a frequency of 1 in 3.2 x 10(3) viable spores. Two t ypes of deletion events giving rise to lys(+) pyr(-) and lys(-) pyr(-) phen otypes were obtained with different frequencies. Southern analysis revealed that gene conversion occurs mainly as a result of crossing over events tha t remove the BamHI frameshift mutation present in one of the repeats. In ly s(-) pyr(-) recombinants, the deletion events do not affect the frameshift mutation in the BamHI site, while lys(+) pyr(-) recombinants showed repair of the BamHI frameshift mutation and the genotype of the parental non-disru pted strain was restored. In summary, deletion events in P. chrysogenum ten d to favor the restoration of the phenotype and genotype characteristic of the parental non-disrupted strain.