Literature DB >> 22431132

A novel amino acid substitution Ala-122-Tyr in ALS confers high-level and broad resistance across ALS-inhibiting herbicides.

Heping Han1, Qin Yu, Edison Purba, Mei Li, Michael Walsh, Shane Friesen, Stephen B Powles.   

Abstract

BACKGROUND: Wild radish, a problem weed worldwide, is a severe dicotyledonous weed in crops. In Australia, sustained reliance on ALS-inhibiting herbicides to control this species has led to the evolution of many resistant populations endowed by any of several ALS mutations. The molecular basis of ALS-inhibiting herbicide resistance in a novel resistant population was studied.
RESULTS: ALS gene sequencing revealed a previously unreported substitution of Tyr for Ala at amino acid position 122 in resistant individuals of a wild radish population (WARR30). A purified subpopulation individually homozygous for the Ala-122-Tyr mutation was generated and characterised in terms of its response to the different chemical classes of ALS-inhibiting herbicides. Whole-plant dose-response studies showed that the purified subpopulation was highly resistant to chlorsulfuron, metosulam and imazamox, with LD₅₀ or GR₅₀ R/S ratio of > 1024, > 512 and > 137 respectively. The resistance to imazypyr was found to be relatively moderate (but still substantial), with LD₅₀ and GR₅₀ R/S ratios of > 16 and > 7.8 respectively. In vitro ALS activity assays showed that Ala-122-Tyr ALS was highly resistant to all tested ALS-inhibiting herbicides.
CONCLUSION: The molecular basis of ALS-inhibiting herbicide resistance in wild radish population WARR30 was identified to be due to an Ala-122-Tyr mutation in the ALS gene. This is the first report of an amino acid substitution at Ala-122 in the plant ALS that confers high-level and broad-spectrum resistance to ALS-inhibiting herbicides, a remarkable contrast to the known mutation Ala-122-Thr endowing resistance to imidazolinone herbicide.
Copyright © 2012 Society of Chemical Industry.

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Year:  2012        PMID: 22431132     DOI: 10.1002/ps.3278

Source DB:  PubMed          Journal:  Pest Manag Sci        ISSN: 1526-498X            Impact factor:   4.845


  8 in total

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Journal:  J Virol       Date:  2014-06-18       Impact factor: 5.103

2.  Genetic characterization of the acetohydroxyacid synthase (AHAS) gene responsible for resistance to imidazolinone in chickpea (Cicer arietinum L.).

Authors:  Courtney Thompson; Bunyamin Tar'an
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3.  A new amino acid substitution (Ala-205-Phe) in acetolactate synthase (ALS) confers broad spectrum resistance to ALS-inhibiting herbicides.

Authors:  James T Brosnan; Jose J Vargas; Gregory K Breeden; Logan Grier; Raphael A Aponte; Stefan Tresch; Martin Laforest
Journal:  Planta       Date:  2015-09-09       Impact factor: 4.116

4.  A New Ala-122-Asn Amino Acid Change Confers Decreased Fitness to ALS-Resistant Echinochloa crus-galli.

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Journal:  Front Plant Sci       Date:  2017-11-28       Impact factor: 5.753

5.  Target-Site Mutations and Expression of ALS Gene Copies Vary According to Echinochloa Species.

Authors:  Silvia Panozzo; Elisa Mascanzoni; Laura Scarabel; Andrea Milani; Giliardi Dalazen; Aldo J Merotto; Patrick J Tranel; Maurizio Sattin
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6.  Multiple Herbicide Resistance in Lolium multiflorum and Identification of Conserved Regulatory Elements of Herbicide Resistance Genes.

Authors:  Khalid Mahmood; Solvejg K Mathiassen; Michael Kristensen; Per Kudsk
Journal:  Front Plant Sci       Date:  2016-08-05       Impact factor: 5.753

7.  Non-target site-based resistance to tribenuron-methyl and essential involved genes in Myosoton aquaticum (L.).

Authors:  Weitang Liu; Shuang Bai; Ning Zhao; Sisi Jia; Wei Li; Lele Zhang; Jinxin Wang
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8.  Target site as the main mechanism of resistance to imazamox in a Euphorbia heterophylla biotype.

Authors:  Antonia M Rojano-Delgado; João M Portugal; Candelario Palma-Bautista; Ricardo Alcántara-de la Cruz; Joel Torra; Esteban Alcántara; Rafael De Prado
Journal:  Sci Rep       Date:  2019-10-28       Impact factor: 4.379

  8 in total

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