Literature DB >> 25472976

Strigolactones contribute to shoot elongation and to the formation of leaf margin serrations in Medicago truncatula R108.

Dominique Lauressergues1, Olivier André1, Jianling Peng2, Jiangqi Wen2, Rujin Chen2, Pascal Ratet3, Million Tadege2, Kirankumar S Mysore2, Soizic F Rochange4.   

Abstract

Strigolactones were recently identified as a new class of plant hormones involved in the control of shoot branching. The characterization of strigolactone mutants in several species has progressively revealed their contribution to several other aspects of development in roots and shoots. In this article, we characterize strigolactone-deficient and strigolactone-insensitive mutants of the model legume Medicago truncatula for aerial developmental traits. The most striking mutant phenotype observed was compact shoot architecture. In contrast with what was reported in other species, this could not be attributed to enhanced shoot branching, but was instead due to reduced shoot elongation. Another notable feature was the modified leaf shape in strigolactone mutants: serrations at the leaf margin were smaller in the mutants than in wild-type plants. This phenotype could be rescued in a dose-dependent manner by exogenous strigolactone treatments of strigolactone-deficient mutants, but not of strigolactone-insensitive mutants. Treatment with the auxin transport inhibitor N-1-naphthylphtalamic acid resulted in smooth leaf margins, opposite to the effect of strigolactone treatment. The contribution of strigolactones to the formation of leaf serrations in M. truncatula R108 line represents a novel function of these hormones, which has not been revealed by the analysis of strigolactone mutants in other species.
© The Author 2014. Published by Oxford University Press on behalf of the Society for Experimental Biology. All rights reserved. For permissions, please email: journals.permissions@oup.com.

Entities:  

Keywords:  Medicago truncatula; elongation; leaf; mutant; phytohormone; shoot; strigolactone.

Mesh:

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Year:  2014        PMID: 25472976      PMCID: PMC4438446          DOI: 10.1093/jxb/eru471

Source DB:  PubMed          Journal:  J Exp Bot        ISSN: 0022-0957            Impact factor:   6.992


  59 in total

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