Expression of the arylsulfatase gene from the beta 2-tubulin promoter in Chlamydomonas reinhardtii.

Abstract:

:Arylsulfatase, produced by Chlamydomonas reinhardtii during sulfur-limited growth, is secreted into the periplasmic space and is readily assayed using a chromogenic substrate. To assess the usefulness of the gene encoding arylsulfatase (ars) as a reporter gene in C. reinhardtii, we have fused the promoter region of the beta 2-tubulin gene (tubB2) to the coding region of an ars genomic clone to form a tubB2/ars chimeric sequence. This construct was introduced into C. reinhardtii, strain CC425 (cw-15, arg-2), via cotransformation with the argininosuccinate lyase gene (which complements the arg-2 lesion) (1). Transformants expressing arylsulfatase (Ars) in sulfur-sufficient medium were isolated and subsequently shown to contain the tubB2/ars gene. RNA analysis determined that tubB2/ars transcripts accumulated in these cells. Abundance of the chimeric transcript increased immediately following deflagellation in a manner similar to that of the endogenous tubB2 transcript. Thus, chimeric genes incorporating ars coding sequences and heterologous promoters can be used to examine regulated gene expression in C. reinhardtii.

journal_name

Nucleic Acids Res

journal_title

Nucleic acids research

authors

Davies JP,Weeks DP,Grossman AR

doi

10.1093/nar/20.12.2959

keywords:

subject

Has Abstract

pub_date

1992-06-25 00:00:00

pages

2959-65

issue

12

eissn

0305-1048

issn

1362-4962

journal_volume

20

pub_type

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