Targeted disruption of the NIT8 gene in Chlamydomonas reinhardtii

Julie A.E. Nelson, Paul A. Lefebvre

Research output: Contribution to journalArticlepeer-review

52 Scopus citations

Abstract

We have used homologous recombination to disrupt the nuclear gene NIT8 in Chlamydomonas reinhardtii. This is the first report of targeted gene disruption of an endogenous locus in C. reinhardtii and only the second for a photosynthetic eukaryote. NIT8 encodes a protein necessary for nitrate and nitrite assimilation by C. reinhardtii. A disruption vector was constructed by placing the CRY1-1 selectable marker gene, which confers emetine resistance, within the NIT8 coding region. nit8 mutants are unable to grow on nitrate as their sole nitrogen source (Nit-) and are resistant to killing by chlorate. One of 2,000 transformants obtained after selection on emetine- chlorate medium contained a homologous insertion of live copies of the disruption plasmid into the NIT8 gene, producing an emetine-resistant, chlorate-resistant Nit- phenotype. The mutant phenotype was rescued by the wild-type NIT8 gene upon transformation. Seven other mutations at the nit8 locus, presumably resulting from homologous recombination with the disruption plasmid, were identified but were shown to be accompanied by deletions of the surrounding genomic region.

Original languageEnglish (US)
Pages (from-to)5762-5769
Number of pages8
JournalMolecular and cellular biology
Volume15
Issue number10
DOIs
StatePublished - Oct 1995

Fingerprint Dive into the research topics of 'Targeted disruption of the NIT8 gene in Chlamydomonas reinhardtii'. Together they form a unique fingerprint.

Cite this