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PMID: 9003322 Published · ppublish English Journal Article Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

Characterization of tryptophan synthase alpha subunit mutants of Arabidopsis thaliana.

Molecular & general genetics : MGG ·Vol. 253 ·No. 3 ·1996-12-13 ·Pages 353-61

Radwanski ER, Barczak AJ, Last RL

Abstract

Three mutations in the Arabidopsis thaliana gene encoding the alpha subunit of tryptophan synthase were isolated by selection for resistance to 5-methylanthranilate or 5-fluoroindole, toxic analogs of tryptophan pathway intermediates. Plants homozygous for trp3-1 and trp3-2 are light-conditional tryptophan auxotrophs, while trp3-100 is a more leaky mutant. Genetic complementation crosses demonstrated that the three mutations are allelic to each other, and define a new complementation group. All three mutants have decreased steady-state levels of tryptophan synthase alpha protein, and the trp3-100 polypeptide exhibits altered electrophoretic mobility. All three mutations were shown to be in the TSA1 (tryptophan synthase alpha subunit) structural gene by several criteria. Firstly, the trp3-1 mutation is linked to TSA1 on the bottom of chromosome 3. Secondly, the trp3-1 mutation was complemented when transformed with the wild-type TSA1 gene. Finally, DNA sequence analysis of the TSA1 gene revealed a single transition mutation in each trp3 mutant.

MeSH Terms
Arabidopsis/enzymology,genetics Chromosome Mapping Mutation Phenotype Plant Proteins/genetics Tryptophan Synthase/genetics,metabolism
Chemicals
Plant Proteins Tryptophan Synthase
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Radwanski E R
Boyce Thompson Institute for Plant Research, Cornell University, Ithaca, NY 14853-1801, USA.
Barczak A J
Last R L
Article Info
Journal
Molecular & general genetics : MGG
Abbr.
Mol Gen Genet
ISSN
0026-8925
Published
1996-12-13
Pages
353-61
Language
English
Region
Germany
NLM ID
0125036
Subset
IM
Grants
NIGMS NIH HHS · GM43134 · United States
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