Integration of genetic, genomic and transcriptomic information identifies putative regulators of adventitious root formation in Populus. Issue 1 (December 2016)

• Record Type: Journal Article
• Authors: Ribeiro, Cintia; Silva, Cynthia; Drost, Derek; Novaes, Evandro; Novaes, Carolina; Dervinis, Christopher; Kirst, Matias
• Is Part Of: BMC plant biology. Volume 16:Issue 1(2016)
• Page Start: 1
• Page End: 11
• Publication Date: 2016-12
• Subjects: Adventitious root -- QTL -- Populus -- SUR2 -- Vegetative propagation; Plant molecular biology -- Periodicals; Botany -- Periodicals; 580.5
• DOI: 10.1186/s12870-016-0753-0
• Languages: English
• ISSNs: 1471-2229

Abstract

Abstract Background Adventitious roots (AR) develop from tissues other than the primary root, in a process physiologically regulated by phytohormones. Adventitious roots provide structural support and contribute to water and nutrient absorption, and are critical for commercial vegetative propagation of several crops. Here we quantified the number of AR, root architectural traits and root biomass in cuttings from a pseudo-backcross population ofPopulus deltoides andPopulus trichocarpa . Quantitative trait loci (QTL) mapping and whole-transcriptome analysis of individuals with alternative QTL alleles for AR number were used to identify putative regulators of AR development. Results Parental individuals and progeny showed extensive segregation for AR developmental traits. Quantitative trait loci for number of AR mapped consistently in the same interval of linkage group (LG) II and LG XIV, explaining 7–10 % of the phenotypic variation. A time series transcriptome analysis identified 26, 121 genes differentially expressed during AR development, particularly during the first 24 h after cuttings were harvested. Of those, 1929 genes were differentially regulated between individuals carrying alternative alleles for the two QTL for number of AR, in one or more time point. Eighty-one of these genes were physically located within the QTL intervals for number of AR, including putative homologs of theArabidopsis genesSUPERROOT2 (SUR2 ) andTRYPTOPHAN SYNTHASE ALPHA CHAIN (TSA1), both of which are involved in the auxin indole-3-acetic acid (IAA) biosynthesis pathway. Conclusions This study suggests the involvement of two genes of the tryptophan-dependent auxin biosynthesis pathway, SUR2 andTSA1, in the regulation of a critical trait for the clonal propagation of woody species. A possible model for this regulation is that poplar individuals that have poor AR formation synthesize auxin indole-3-acetic acid (IAA) primarily through the tryptophan (Trp) pathway. Much of the Trp pathway flux appears to be directed to the synthesis of indole glucosinolates (IG), as suggested by the over-expression ofSUR2 . Individuals that are efficient in AR formation may utilize alternative (non-Trp) pathways to synthesize IAA, based on the observation that they down-regulate the expression ofTSA1, one of the critical steps in the synthesis of tryptophan.