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Protist ; 158(4): 435-46, 2007 Oct.
Article in English | MEDLINE | ID: mdl-17611150

ABSTRACT

Chlamydomonas reinhardtii arg7-8 (arg2) mutant strains carrying a hitherto undescribed mutation in their argininosuccinate lyase gene (ARG7) that leads to arginine auxotrophy have been used together with the corresponding wild-type gene as a very reliable transformation system since 1989. In this study, we finally identify the molecular nature of the arg7-8 mutation as a (6073)G to A transition in exon 9 of ARG7 leading to a (288)Gly to Ser exchange near the active site of the protein. The same mutation was found in the ARG7 genes of three commonly used C. reinhardtii laboratory strains, namely cw15-302 arg2, CC-48, and CC-1618. We did not observe exact spontaneous reversion of the arg7-8 allele in our study, but did identify two different and rare intragenic suppressor mutations, (27)Leu to Phe and (285)Tyr to Phe. In our hands, only transformation of the arg7-8 strain with a truncated nonfunctional wild-type ARG7 gene lacking 124 codons at its 5' end led to exact reversion of the mutant base (6073)A to the wild-type (6073)G, presumably by recombination. This system offers a positive selection scheme for homologous recombination (HR) and may, therefore, be useful to the methodical improvement of recombination in Chlamydomonas.


Subject(s)
Argininosuccinate Lyase/genetics , Chlamydomonas reinhardtii/genetics , Genetic Complementation Test , Point Mutation , Protozoan Proteins/genetics , Sequence Deletion , Alleles , Amino Acid Substitution/genetics , Animals , Binding Sites/genetics , Chlamydomonas reinhardtii/enzymology , Recombination, Genetic , Suppression, Genetic , Transformation, Genetic
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