Theoretical and Applied Genetics

, Volume 118, Issue 2, pp 295–303

Genomic regions influencing gene expression of the HMW glutenins in wheat

  • Eric W. Storlie
  • Robert J. Ihry
  • Leslie M. Baehr
  • Karissa A. Tieszen
  • Jonathan H. Engbers
  • Jordan M. Anderson-Daniels
  • Elizabeth M. Davis
  • Anne G. Gilbertson
  • Niels R. Harden
  • Kristina A. Harris
  • Amanda J. Johnson
  • Amy M. Kerkvleit
  • Matthew M. Moldan
  • Megan E. Bell
  • Michael K. Wanous
Open AccessOriginal Paper

DOI: 10.1007/s00122-008-0899-8

Cite this article as:
Storlie, E.W., Ihry, R.J., Baehr, L.M. et al. Theor Appl Genet (2009) 118: 295. doi:10.1007/s00122-008-0899-8

Abstract

Bread wheat (Triticum aestivum L.) produces glutenin storage proteins in the endosperm. The HMW glutenins confer distinct viscoelastic properties to bread dough. The genetics of HMW glutenin proteins have been extensively studied, and information has accumulated about individual subunits, chromosomal locations and DNA sequences, but little is known about the regulators of the HMW glutenins. This investigation addressed the question of glutenin regulators. Expression of the glutenins was analyzed using QRT-PCR in ditelosomic (dt) Chinese Spring (CS) lines. Primers were designed for each of 4 CS glutenin genes and a control, non-storage protein endosperm-specific gene Agp-L (ADP-glucose pyrophosphorylase). Each line represents CS wheat, lacking one chromosome arm. The effect of a missing arm could feasibly cause an increase, decrease or no change in expression. For each HMW glutenin, results indicated there were, on average, 8 chromosome arms with an up-regulatory effect and only one instance of a down-regulatory effect. There were significant correlations between orthologous and paralogous HMW glutenins for effects of chromosome groups B and D. Some or all the glutenin alleles shared regulatory loci on chromosome arms 2BS, 7BS, 4DS, 5DS and 6DS, and Agp-L shared regulatory loci with glutenins on arms 7AS, 7BS, 2DS, 3DS, 4DS and 5DS. These results suggest a few chromosome arms contain putative regulatory genes affecting the expression of conserved cis elements of 4 HMW glutenin and Agp-L genes in CS. Regulation by common genes implies the regulators have diverged little from the common wheat ancestor, and furthermore, some regulation may be shared by endosperm-specific-genes. Significant common regulators have practical implications.

Introduction

Wheat is an allohexaploid crop plant belonging to the grass (Poaceae) family. Hexaploid wheat consists of three genomes—A, B and D—produced by relatively recent polyploidization events. Each genome is homoeologous to the other genomes and consists of very similar orthologous loci. Gu et al. (2004) suggest the A and D genomes were derived from a common ancestor after separation of the B genome species. Subsequently, the A and B genomes were united when an A genome donor, T. urartu, crossed with an unknown B genome donor and produced T. turgidum. A couple hundred thousand years later T. turgidum crossed with a D genome donor, T. tauschii, and produced T. aestivum (Feldman et al. 1995).

Unusual cytological events resulted in duplicated genomes and loci, including paralogous genes residing on the same chromosomes as the original loci. Duplicated loci may facilitate the plasticity and evolution of an organism by retaining the original function of a gene while allowing its paralog and ortholog to take on modified or novel functions (see reviews by RA Veitia 2005; Adams and Wendel 2005).

Wheat grain consists of starch (70%), protein (11%), fatty acids (3%), ash (2%), and fiber (1.5%) (Clydesdale 1994). Storage proteins, glutenins and gliadins, are synthesized in the endosperm during the grain-filling period; they comprise 90% of the protein in the wheat grain (Huebner and Wall 1974; Pike and MacRitchie 2004). High molecular weight (HMW) glutenin subunits each contribute about 2% of the total seed protein (Payne et al. 1984; Halford et al. 1992) and contribute the unique elastic properties and quality of bread dough.

The HMW glutenins are encoded by loci on homoeologous chromosomes 1L. There are two closely linked paralogous genes, designated Glu-1-1 and Glu-1-2, on chromosomes 1AL, 1BL and 1DL, resulting from an ancestral duplication event. The glutenin genes probably evolved from a single ancestral gene (Kreis et al. 1985). The Glu-1-1 and Glu-1-2 orthologs share more DNA sequence homology than the paralogs (Allaby et al. 1999). The genes Glu-1-1 and Glu-1-2 encode X (high Mr) and Y (low Mr) glutenins, respectively. Two genes are inactive in many cultivars; Chinese Spring (cv) has two inactive genes on chromosome 1AL. The HMW glutenin genes occupying each locus have been cloned and characterized from each homoeologous chromosome (see review by Shewry et al. 2003).

Allelic variation for the active genes translates to HMW glutenin subunit variation. The various subunits have been genetically characterized and correlated with quality characteristics (Payne 1987). Some subunit combinations have a more favorable effect on quality than other combinations. Qualitative factors contributing elastic properties of bread dough may be the regularly occurring β-turns of HMW glutenin polypeptides (Shewry et al. 1989) and tyrosine bonds (Tilley et al. 2001). A quantitative factor contributing to quality includes the proportion of HMW glutenins in relation to other endosperm components (Huebner and Wall 1974; Field et al. 1983; Lawrence et al. 1988). Rooke et al. (1999) analyzed flour from wheat transformed to produce a higher proportion of HMW glutenins; results indicated increased dough strength.

Expression of the HMW glutenin genes determines the content level of subunits. Kolster et al. (1993) analyzed the expression of alleles for Glu-A1, Glu-B1 and Glu-D1 from various donors in a common genetic background, near-isogenic lines, and results indicated the background did not affect subunit ratios. Genetic background did affect properties of bread quality in an experiment involving four doubled haploid wheat populations (Killerman and Zimmerman 2000). Kolster et al. (1993) suggest glutenin loci share a common regulatory mechanism. The suggestion of a common mechanism implies common cis and trans regulators control the expression of glutenin alleles relatively the same, regardless of the genotype. However, an investigation by Thiellement et al. (1986) suggested the duplicated glutenin genes do not share regulation.

The cis regions of the HMW glutenins are conserved 1,200 bp upstream of the start codon and 200–400 bp downstream of the stop codon (Anderson et al. 1998). Lamacchia et al. (2001) indicate the promoter sequence of 1,191 bp upstream of the start site regulates endosperm-specific expression. The upstream promoter regions consist of elements common to grasses in Poideae, prominently including an endosperm box—a GCN4-like motif (GLM, 5′-ATGAG/CTCAT-3′) and a prolamin box (5′-TGTAAAG-3′) (Forde et al. 1985)—a AACA motif (Diaz et al. 2002) and an enhancer element, more specific to HMW glutenins (Thomas and Flavell 1990). Anderson et al. (2002) characterized 5′ and 3′ DNA of HMW glutenins and identified potential matrix-attachment regions (MARs), transposable elements (MITEs), and retrotransposons (LTR and non-LTR) flanking respective glutenin genes. Proposed transcription factors recognize conserved elements of glutenin promoters: the storage protein activator (SPA), a seed-specific basic leucine zipper protein, bZIP (Albani et al. 1997), DNA binding with one finger (Dof) prolamin box binding factor (Vicente-Carbajosa et al. 1997) and a MYB-protein, possibly interacting with the Dof protein (Diaz et al. 2002). Wheat and other cereals share cis motifs and trans domains for the regulation of storage and possibly other proteins.

Approaches to the identification and mapping of regulators have included genetic mapping using aneuploid wheat (Galili and Feldman 1985; Rogers et al. 1990; Wanous et al. 2003) and genetic linkage analysis using wheat populations (Guillaumie et al. 2004). Guillaumie et al. (2004) genetically mapped SPA to the long arm of chromosome 1B, and Ravel et al. (2006) mapped Dof to the long arm of chromosome 5. Wanous et al. (2003) analyzed HMW glutenin proteins in ditelosomic wheat lines, and results indicated genes on several chromosome arms affected the regulation of each glutenin.

Regulation of gene expression may feasibly occur at any point between transcription and protein functionality. Some investigations suggest regulation of HMW glutenins occurs primarily at the transcriptional level (Bartels and Thompson 1986; Sorensen et al. 1989).

One objective of this investigation was to analyze HMW glutenin gene expression in ditelosomic wheat lines and to correlate these results with a previous study on protein expression (Wanous et al. 2003) and to determine if glutenins are regulated mostly at the transcriptional or post-transcriptional levels. Another objective was to correlate expression of orthologous and paralogous glutenin genes affected by the chromosome groups for indications of common chromosomal locations of glutenin regulation. The glutenin genes provide a unique set of genes to study the regulatory effects of duplicated genes in a polyploid plant. Also, common locations may contain important regulatory alleles contributing content level variation for the HMW subunits. Manipulation of this variation with molecular biological tools may facilitate plant selections for favorable qualities (Rathmell et al. 2001). A control, non-storage protein, endosperm-specific gene, Agp-L, was included for an indication of the specificity—tissue or protein class—of gene expression.

Materials and methods

Plant material

Sears (1954) produced ditelosomic (dt) Chinese Spring wheat lines. For chromosome arms where dt lines were available, dt endosperm was compared to euploid CS seeds (0 vs. 3 doses in the endosperm). For chromosome arms where dt lines were not available, tetrasomic endosperm was compared to euploid CS endosperm (6 vs. 3 doses). CS and related aneuploid lines were obtained from the University of Missouri—Columbia. Three replicates of each CS euploid and aneuploid line were grown in 6′′-diameter pots filled with commercial potting soil. The growth chamber conditions were set at 25°C, 14 h of light from incandescent and metal halide lamps. The soil was saturated with water once a day and 1.0 g of Osmocote (Maryville, OH, USA) fertilizer applied to each plant, every 4 weeks.

Seed harvest and RNA extraction

Seeds were harvested 15 days post-anthesis (dpa). The embryo and pericarp were removed and the endosperm was placed in a microfuge tube and immersed in liquid N and subsequently stored at −70°C, until further processing. The endosperm was ground with mortar and pestle, frozen with liquid N. RNA was extracted using a modified Trizol (Invitrogen; Carlsbad, CA, USA) protocol. The RNA sample was treated with DNase and purified with Qiagen RNeasy kit (Germany). Samples were quantified and protein contamination estimated using a Hitachi spectrophotometer (Japan) and separated on a 1% agarose gel for an evaluation of degradation. Samples were stored at −20°C until analysis.

Primer design

HMW glutenin nucleotide sequences were acquired from GenBank and aligned using MegAlign software (DNA*, Madison, WI, USA). Primers were designed for each glutenin gene based on nucleotide differences that distinguished each glutenin from the other three.

Genome specific primer design for the large subunit of ADP-glucose pyrophosphorylase (Agp-L) was executed by creating primers from a consensus sequence of Agp-L GenBank accessions X66080, AF244997, EF405961 and AF492644. The primers amplified a 649 bp fragment from diploid wheat progenitors: Triticum monococcum (genome donor, A), Aegilops speltoides (genome donor, B), and Triticum tauschii (genome donor, D). Amplicons from the progenitors were then sequenced.

These sequences were aligned to compare sequences from each genome. The alignment revealed genome specific single-nucleotide-polymorphisms (SNPs) for each genome and provided the basis for the design of an A genome specific Agp-L primer pair. An Agp-L primer pair designed for the A genome was confirmed to be genome specific by comparing presence and absence of amplicons between euploid CS and Dt1AS. The absence of an amplicon in the Dt1AS sample suggests the specificity of primers and chromosome location of Agp-L within the A genome, on the long arm of chromosome 1A. Primer sequences (5′–3′) for the housekeeping gene, 18S rRNA, control, Agp-L and HMW glutenins:
  • Agp-L consensus:

  • Forward, AAGCGATGAAAGTGGACACC

  • Reverse, CTTCTTGCACTCCCTCCTTG

  • (amplicon size = 649 bp)

  • Agp-L (A-genome specific):

  • Forward, TATATTGCGTCGATGGGAG

  • Reverse, ATTCAAACTTTGGAGGCTG

  • (amplicon size = 229 bp)

  • 18S rRNA:

  • Forward, CTGGGAGGGGCGCATTTATTAGAT

  • Reverse, CCCGGCCCAAGGTCCAACT

  • (amplicon size = 463 bp)

  • Glu-B1-1:

  • Forward, TAAGCGCCTGGTCCTCTTTG

  • Reverse, CACCTGTTGGCATGCCTC

  • (amplicon size = 118 bp)

  • Glu-B1-2:

  • Forward, CGACAACCCATACCATGTTAACAC

  • Reverse, GGGTTGCTGCACCTTTGCC

  • (amplicon size = 70 bp)

  • Glu-D1-1:

  • Forward, GTCGCGGGACAATACGAG

  • Reverse, GTGCAGGTATTCCCCAAAATATAC

  • (amplicon size = 118 bp)

  • Glu-D1-2:

  • Forward, GCCAAGTGCCGCTCCGTC

  • Reverse, TGGTCTCACCAGGGTAGAAGGATCC

  • (amplicon size = 102 bp)

QRT-PCR

A quantitative RT-PCR method estimated Cycle threshold (Ct) values, using a Cepheid SmartCycler II thermocycler (Sunnyvale, CA, USA), from the endosperm RNA. The Ct values of HMW glutenin and Agp-L genes were normalized with Ct values of 18S rRNA. All samples were replicated three times. An expression ratio was calculated from the normalized control, euploid CS, and the normalized samples, ditelosomic or tetrasomic CS. Significance was determined with P-values (< 0.05) estimated from the “Pair Wise Fixed Reallocation Randomization Test,” derived from the “Relative Expression Software Tool” (Pfaffl et al. 2001).

Correlation analysis

SPSS 12.1 (Chicago, IL, USA) was used to estimate Spearman’s correlations (r) of expression between HMW glutenin alleles.

Results

Quantitative RT-PCR was used to analyze the HMW glutenin gene expression of CS euploid and ditelosomic wheat lines for an estimate of chromosomal locations having a significant effect. Expression of HMW glutenins and Agp-L genes was significantly affected by putative regulatory genes residing on several chromosome arms (Fig. 1, Table 1). Expression of the Agp-L and each HMW glutenin gene was up-regulated by putative genes on 5–13 chromosome arms (Fig. 1; Table 1). In only one instance, for Glu-D1-2, was expression down-regulated by a gene(s) on 1DS. This observation is consistent with previous studies indicating the expression of structural genes is commonly influenced by multiple dosage sensitive regulatory loci (Guo and Birchler 1994). Gene expression was most significantly affected by 1AL, 1BL and 1DL for Agp-L, Glu-B1 and Glu-D1, respectively, where these loci reside. In a previous study, Wanous et al. (2003) showed chromosomes 1BL and 1DL had the most significant effects on Glu-B1 and Glu-D1 protein expression. The corresponding results of these studies and a preceding investigation by Greene (1983) suggest HMW glutenin RNA transcript levels predict the final protein concentration and confirm the consistency and reliability of ditelosomic genetic stocks for expression analysis.
Table 1

Relative gene expression of HMW glutenins and Agp-L in ditelosomic wheat revealed chromosome arms where putative regulatory genes reside

https://static-content.springer.com/image/art%3A10.1007%2Fs00122-008-0899-8/MediaObjects/122_2008_899_Tab1_HTML.gif

The HMW glutenin, Agp-L and 18S rRNA genes are depicted in the first column to the left and are repeated in three groups, one for each chromosome—A, B and D. Significant regulatory effects of a chromosome arm are depicted as a factor of increased or decreased expression caused by a putative regulator residing on the chromosome arm. Significant regulatory effects on paralogs or orthologs and shared by Agp-L are highlighted in gray. Regulation was up or down relative to euploid CS and a housekeeping gene, 18S rRNA. Relative expression was estimated from an expression ratio \( \left[ {2_{\text{target}}^{{(C_{{{\text{t}}\,{\text{control}}}} - C_{{{\text{t}}\,{\text{sample}}}} )}} /2_{\text{reference}}^{{(C_{{{\text{t}}\,{\text{control}}}} - C_{{{\text{t}}\,{\text{sample}}}} )}} } \right] \)

The HMW glutenin genes shared effects of putative regulatory loci on groups B and D, based on strong correlations of expression effects of group B and D chromosome arms. Chromosome arms 2BS, 7BS and 5DS had significant up-regulatory effects on each of the glutenin genes; chromosome arm 4DS had significant effects on all glutenins, except Glu-D1-1; chromosome arm 6DS had significant effects on the paralogous genes, Glu-B1-1 and Glu-B1-2; chromosome arm 2DS had significant effects on the paralogous genes, Glu-B1-1 and Glu-D1-2 (Fig. 1). Chromosome arms 7BS, 2DS, 4DS and 5DS also had up-regulatory effects on the control gene, Agp-L (Fig. 1).
https://static-content.springer.com/image/art%3A10.1007%2Fs00122-008-0899-8/MediaObjects/122_2008_899_Fig1_HTML.gif
Fig. 1

Relative gene expression of HMW glutenins in ditelosomic wheat revealed chromosome arms where putative regulatory genes reside. Regulation was estimated as up or down regulated relative to euploid CS and a housekeeping gene, 18S rRNA. Relative expression was estimated from an expression ratio\( \left[ {2_{\text{target}}^{{(C_{{{\text{t}}\,{\text{control}}}} - C_{{{\text{t}}\,{\text{sample}}}} )}} /2_{\text{reference}}^{{(C_{{{\text{t}}\,{\text{control}}}} - C_{{{\text{t}}\,{\text{sample}}}} )}} } \right]. \) Each graph depicts the effects of chromosome arms 1L-7S for each chromosome group—A (graph a) B (graph b) and D (graph c)—on expression of Glu-B1-1, Glu-B1-2, Glu-D1-1, and Glu-D1-2 and a control, non-storage protein gene, Agp-L. These genes are encoded on chromosome 1L, and the graphics for the effects of these chromosome arms represent up or down regulation of the loci

The regulation of orthologous and paralogous genes may be shared, independent or both, depending on the evolution of cis elements and trans factors. There were significant correlations between orthologous and paralogous HMW glutenins for effects of chromosome groups B and D (Table 2). The correlations include the effects of all chromosome arms of a chromosome group, except the glutenin locus on 1L (Table 2). A correlation between glutenin gene expression indicates significant correlations (< 0.01) for all possible pairs of Glu-B1 and Glu-D1 for effects of chromosome group B (Table 2; Fig. 1b). The orthologs Glu-B1-1:Glu-D1-1 and Glu-B1-2:Glu-D1-2 and the paralogs Glu-B1-1:Glu-B1-2, Glu-B1-1:Glu-D1-2, Glu-B1-2:Glu-D1-1 and Glu-D1-1:Glu-D1-2 shared effects of chromosome group B arms (Table 2). There was one significant correlation (P < 0.01) for effects of chromosome group D on the paralogs Glu-B1-1 and Glu-B1-2 and on the glutenin gene, Glu-D1-2, and the control gene, Agp-L (Table 2; Fig. 1c). There were no significant correlations for any gene pairs for effects of chromosome group A or for effects of homoeologous chromosome groups—A:B, A:D or B:D—though there were instances of shared expression effects of 2BS:2DS, 3AL:3DL, 6AL:6DL, 6AS:6DS and 7AS:7BS on some glutenin genes (Table 1), and there were some instances of individual, non-shared effects of chromosome arms—3AL, 7BL, 1DS, 3DL and 3DS—on single glutenin genes (Table 1).
Table 2

Bivariate correlations for the expression of HMW glutenin (Glu-B1-1, Glu-B1-2, Glu-D1-1 and Glu-D1-2) and Agp-L gene expression in CS wheat

https://static-content.springer.com/image/art%3A10.1007%2Fs00122-008-0899-8/MediaObjects/122_2008_899_Tab2_HTML.gif

Expression as depicted in Fig. 1 and Table 1 (except data for chromosomes 1L because the structural gene effects overwhelm the detection of some correlations of expression on other chromosome arms) was correlated in all possible combinations. Significant correlations are depicted in bold with asterisks. Expression ratios for each gene were correlated with each other in all possible combinations using Spearman’s correlation. The expression data for each glutenin and Agp-L gene analyzed for all chromosome arms of a chromosome group—A, B and D—were included in each correlation. Significant correlations are highlighted in bold with backgrounds of white or gray

Discussion

The HMW glutenin gene expression on chromosomes 1BL and 1DL corresponds with the protein expression results (Wanous et al. 2003), confirming the methods of protein and mRNA quantification. There were no overall correlations (P > 0.05) between glutenin genes and proteins for effects of respective chromosome groups on expression; chromosome arms of each chromosome group uniquely affected gene and protein regulation. The difference between the putative regulatory genes for protein and gene expression are summarized for up and down regulation: glutenin protein expression was up-regulated by putative trans regulators on 10 chromosome arms and down-regulated by regulators on 5 chromosome arms, on average (protein data from Wanous et al. 2003); glutenin genes were up-regulated by putative trans regulators on 8, on average, and down-regulated by 1, only, chromosome arm(s). However, about 29% of the positive effects seen at the protein level (Wanous et al. 2003) also showed positive effects on transcript abundance in this study. These interactions include the positive effects of 2DS on Glu-B1-1 and Glu-D1-2; 2BS on Glu-B1-2, Glu-D1-1 and Glu-D1-2; 5DS on Glu-B1-1 and Glu-D1-1; 6DS on Glu-B1-2; 6DL on Glu-B1-1; 6AL on Glu-D1-1; and 7BS on Glu-D1-2. These differences suggest HMW glutenin regulation occurs at various points between gene transcription and protein function; the HMW glutenin proteins probably undergo translational and post-translational control.

Ancient and relatively recent cytological events were responsible for the duplication of HMW glutenin genes resulting in paralogs and orthologs. One objective of this study was to compare the expression patterns of orthologous and paralogous HMW glutenin genes for implications of shared regulatory elements. Results indicate cis and trans elements on chromosome groups B and D are shared between paralogous and orthologous glutenins. There is no indication from this data that one duplication type was more conserved. Previous investigations have shown the orthologs are more highly conserved than the paralogs (Allaby et al. 1999; Anderson et al. 2002). Correlations between all combinations of glutenins and the control genes suggest chromosome group B has a common regulatory effect on glutenin paralogs and orthologs but not the control; group D had a common effect on Glu-B1-1:Glu-B1-2 and Glu-D1-2:Agp-L. The same chromosome group, rather than homoeologs, was involved with common regulatory effects; trans elements of one chromosome group had similar effects on the cis elements of several paralogs, orthologs and between one glutenin and Agp-L. Duplication of trans regulators on homoelogous chromosome arms was suggested for five chromosome arms—2S, 3L, 6L, 6S and 7S—but shared regulation between homoeologs was minimal.

It has been hypothesized that aneuploid conditions may reduce vigor of an organism due to an imbalance of gene products expressed from the affected chromosome. Guo and Birchler (1994) conclude transcript levels for most genes maintained a constant level regardless of the chromosome dosage; regulatory genes were probably involved with the compensation of transcript levels of structural genes affected by chromosome dosage, increase or decrease. Guo and Birchler (1994) suggest the imbalance is a result of an altered regulatory system. In maize, Guo and Birchler (1994) identified 4 chromosomal regions with significant regulatory effects on the storage protein, Zein and 8 chromosomal regions with effects on Shrunken 1, Sucrose Synthase. The many regulators are part of a strict spatial and temporal development of specialized tissues. For example, Glu-B1-1 and Agp-L were differentially expressed in the root compared with the grain tissue (Laudencia-Chingcuanco et al. 2006).

A conserved promoter sequence (Anderson et al. 1998) elicited a common response to putative regulators on certain chromosome arms; in many instances, putative regulators had an up-regulatory effect on an ancestral cis element retained by each orthologous and paralogous glutenin and Agp-L. Potential cis elements include the endosperm box, an AACA motif and an enhancer element (Forde et al. 1985; Thomas and Flavell 1990; Diaz et al. 2002). The common effect on the retained cis elements was initiated by putative trans factors residing on chromosomes 2BS, 7BS, 4DS, 5DS and 6DS. Potential transcription factors include the SPA, a seed-specific basic leucine zipper protein, bZIP, Dof prolamin box binding factor and a MYB-protein, possibly interacting with the Dof protein (Albani et al. 1997; Vicente-Carbajosa et al. 1997; Diaz et al. 2002). Trans factors on the homoeologous chromosome arms did not produce the same effects (though there are other, minor examples in Table 1—2BS:2DS, 3AL:3DL, 6AL:6DL, 6AS:6DS and 7AS:7BS—of possible shared homoeologous trans regulators). After polyploidization, most orthologous trans factors may have been silenced due to an inefficient redundancy (see review by Wolfe 2001). Kashkush et al. (2002) analyzed F1 intergeneric Triticeae hybrids for alterations of gene structure and expression: results indicate genetic and epigenetic changes occurred at the F1 stage, causing gene loss, silencing and activation. Gu et al. (2004) elucidated possible mechanisms of gene silencing in wheat and concluded retrotransposon insertions were a primary cause. After gene duplication events, wheat has retained the functionality of some genes and silenced others. Anderson et al. (2002) identified transposable element and retrotransposon sequences in the flanking regions of HMW glutenins and suggest these were a mechanism of sequence divergence after the initial duplication event. The HMW glutenin and Agp-L genes have revealed shared regulation of duplicated and tissue-specific genes: hypothetically, cis regulatory elements of the glutenin paralogs, orthologs and Agp-L share the recognition of trans regulators on several chromosome arms (Fig. 1; Table 1).

Results of this investigation suggest a few chromosome arms contain regulatory genes affecting expression of 4 HMW glutenin and Agp-L genes. Regulation by common genes implies the work involved with identification of important regulatory genes is simplified and worthwhile. Notably, putative genes on chromosomes 2BS, 7BS and 5DS controlled a significant level of regulation for each paralogous and orthologous glutenin gene. Putative genes on 4DS and 6DS controlled regulation for some paralogous and orthologous glutenins. Genes controlling expression may be identified in a mapping study that isolates regions of these chromosome arms conferring variation for glutenin protein. Previous investigations have identified the chromosomal location of storage protein regulators (Guillaumie et al. 2004; Prasad et al. 1999; Colas des Frances and Thiellement 1985). Guillaumie et al. (2004) mapped SPA to chromosome group 1L, the same chromosomal arm as the HMW glutenin structural genes. Perretant et al. (2000) mapped bread-making quality and identified QTLs for dough strength on chromosomes 5D, 1A and 3B. Ravel et al. (2006) mapped Dof on chromosome 5L. Putative regulator(s) on chromosome 5DS were important for expression of all the HMW glutenins. The isolated regions may reveal candidate regulatory genes in the bin maps available at GrainGenes. Candidate genes and molecular markers may be used in breeding programs to improve the glutenin protein and, possibly, starch composition of wheat.

Evolutionary duplication events produced novel Triticum species with multiple loci of HMW glutenin genes. These genes have been well characterized and provide a unique opportunity to investigate gene expression effects of a polyploid genome on orthologous and paralogous genes. Hypothetically, there are several potential cis and trans regulatory adaptations, and this study provides insight into an example of how a polyploid plant conserved cis regulatory elements of active orthologs and paralogs (two previously investigated inactive glutenins on 1AL were caused by a relatively recent genetic or epigenetic alteration) and silenced redundant trans factors on most homoeologous chromosome arms. There were a few instances of independent regulators affecting the expression of one glutenin gene, and in most instances, putative regulators from one chromosome arm were shared by orthologs and paralogs. Shared regulation between glutenins and other endosperm-specific genes—Agp-L-residing on different genomes—B or D—implies the cis and trans regulators did not diverge extensively from the common ancestor through the evolution and development of modern wheat.

Acknowledgments

EWS, RJI, LMB, KAT, AGG, AJJ, MMM, and MKW were supported by NIH grant 2 P20 RR016479 from the INBRE Program of the National Center for Research Resources. LMB, JHE, JMA, EMD, and KAH were supported by the National Research Initiative of the USDA CSREES, grant 2003-35301-13216. NRH and AMK were supported by NSF EPSCoR grant 0091948 and by the State of South Dakota. RJI was supported by the NASA South Dakota Space Grant Consortium. We thank the reviewers for their comments.

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Authors and Affiliations

  • Eric W. Storlie
    • 1
  • Robert J. Ihry
    • 2
  • Leslie M. Baehr
    • 3
  • Karissa A. Tieszen
    • 2
  • Jonathan H. Engbers
    • 4
  • Jordan M. Anderson-Daniels
    • 1
  • Elizabeth M. Davis
    • 5
  • Anne G. Gilbertson
    • 1
  • Niels R. Harden
    • 6
  • Kristina A. Harris
    • 7
  • Amanda J. Johnson
    • 8
  • Amy M. Kerkvleit
    • 9
  • Matthew M. Moldan
    • 1
  • Megan E. Bell
    • 10
  • Michael K. Wanous
    • 1
  1. 1.Department of BiologyAugustana CollegeSioux FallsUSA
  2. 2.Cell and Molecular Biology ProgramUniversity of WisconsinMadisonUSA
  3. 3.Section of Neurobiology, Physiology, and BehaviorUniversity of CaliforniaDavisUSA
  4. 4.Carver College of MedicineUniversity of IowaIowaUSA
  5. 5.Sanford School of MedicineUniversity of South DakotaVermillionUSA
  6. 6.Mayo School of Graduate Medical EducationRochesterUSA
  7. 7.Department of Nutritional SciencesPennsylvania State UniversityUniversity ParkUSA
  8. 8.University of North Dakota School of Medicine & Health SciencesGrand ForksUSA
  9. 9.Creighton University School of MedicineOmahaUSA
  10. 10.Biology DepartmentBethel UniversitySt PaulUSA