TY - JOUR
T1 - Genome distribution of differential homoeologue contributions to leaf gene expression in bread wheat
AU - Harper, Andrea Louise
AU - Trick, Martin
AU - He, Zhesi
AU - Clissold, Leah
AU - Fellgett, Alison
AU - Griffiths, Simon
AU - Bancroft, Ian
N1 - © 2015 The Authors. This content is made available by the publisher under a Creative Commons CC BY Licence
PY - 2015
Y1 - 2015
N2 - Using a combination of de novo transcriptome assembly, a newly-developed 9495-marker transcriptome SNP genetic linkage map and comparative genomics approaches, we developed an ordered set of non-redundant transcripts for each of the sub-genomes of hexaploid wheat: A (47,160 unigenes), B (59,663 unigenes) and D (40,588 unigenes). We used these as reference sequences against which to map Illumina mRNA-seq reads derived from young leaf tissue. Transcript abundance was quantified for each unigene. Using a 3-way reciprocal BLAST approach, 15,527 triplet sets of homoeologues (one from each genome) were identified. Differential expression (P<0.05) was identified for 5,248 unigenes, with 2906 represented at greater abundance than their two homoeologues and 2342 represented at lower abundance than their two homoeologues. Analysis of gene ontology terms revealed no biases between homoeologues. There was no evidence of genome-wide dominance effects, rather the more highly transcribed individual genes were distributed throughout all three genomes. Transcriptome Display Tile Plot (TDTP), a visualization approach based on CMYK colourspace, was developed and used to assess the genome for regions of skewed homoeologue transcript abundance. Extensive striation was revealed, indicative of many small regions of genome dominance (transcripts of homoeologues from one genome more abundant than the others) and many larger regions of genome repression (transcripts of homoeologues from one genome less abundant than the others).
AB - Using a combination of de novo transcriptome assembly, a newly-developed 9495-marker transcriptome SNP genetic linkage map and comparative genomics approaches, we developed an ordered set of non-redundant transcripts for each of the sub-genomes of hexaploid wheat: A (47,160 unigenes), B (59,663 unigenes) and D (40,588 unigenes). We used these as reference sequences against which to map Illumina mRNA-seq reads derived from young leaf tissue. Transcript abundance was quantified for each unigene. Using a 3-way reciprocal BLAST approach, 15,527 triplet sets of homoeologues (one from each genome) were identified. Differential expression (P<0.05) was identified for 5,248 unigenes, with 2906 represented at greater abundance than their two homoeologues and 2342 represented at lower abundance than their two homoeologues. Analysis of gene ontology terms revealed no biases between homoeologues. There was no evidence of genome-wide dominance effects, rather the more highly transcribed individual genes were distributed throughout all three genomes. Transcriptome Display Tile Plot (TDTP), a visualization approach based on CMYK colourspace, was developed and used to assess the genome for regions of skewed homoeologue transcript abundance. Extensive striation was revealed, indicative of many small regions of genome dominance (transcripts of homoeologues from one genome more abundant than the others) and many larger regions of genome repression (transcripts of homoeologues from one genome less abundant than the others).
U2 - 10.1111/pbi.12486
DO - 10.1111/pbi.12486
M3 - Article
SN - 1467-7644
JO - Plant biotechnology journal
JF - Plant biotechnology journal
ER -