The barley amo1 locus is tightly linked to the starch synthase IIIa gene and negatively regulates expression of granule-bound starch synthetic genes
In this study of barley starch synthesis, the interaction between mutations at the sex6 locus and the amo1 locus has been characterized. Four barley genotypes, the wild type, sex6, amo1, and the amo1sex6 double mutant, were generated by backcrossing the sex6 mutation present in Himalaya292 into the...
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Published in | Journal of experimental botany Vol. 62; no. 14; pp. 5217 - 5231 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
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Oxford University Press
01.10.2011
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Abstract | In this study of barley starch synthesis, the interaction between mutations at the sex6 locus and the amo1 locus has been characterized. Four barley genotypes, the wild type, sex6, amo1, and the amo1sex6 double mutant, were generated by backcrossing the sex6 mutation present in Himalaya292 into the amo1 'high amylose Glacier'. The wild type, amo1, and sex6 genotypes gave starch phenotypes consistent with previous studies. However, the amo1sex6 double mutant yielded an unexpected phenotype, a significant increase in starch content relative to the sex6 phenotype. Amylose content (as a percentage of starch) was not increased above the level observed for the sex6 mutation alone; however, on a per seed basis, grain from lines containing the amo1 mutation (amo1 mutants and amo1sex6 double mutants) synthesize significantly more amylose than the wild-type lines and sex6 mutants. The level of granule-bound starch synthase I (GBSSI) protein in starch granules is increased in lines containing the amo1 mutation (amo1 and amo1sex6). In the amo1 genotype, starch synthase I (SSI), SSIIa, starch branching enzyme IIa (SBEIIa), and SBEIIb also markedly increased in the starch granules. Genetic mapping studies indicate that the ssIIIa gene is tightly linked to the amo1 locus, and the SSIIIa protein from the amo1 mutant has a leucine to arginine residue substitution in a conserved domain. Zymogram analysis indicates that the amo1 phenotype is not a consequence of total loss of enzymatic activity although it remains possible that the amo1 phenotype is underpinned by a more subtle change. It is therefore proposed that amo1 may be a negative regulator of other genes of starch synthesis. |
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AbstractList | In this study of barley starch synthesis, the interaction between mutations at the sex6 locus and the amo1 locus has been characterized. Four barley genotypes, the wild type, sex6, amo1, and the amo1sex6 double mutant, were generated by backcrossing the sex6 mutation present in Himalaya292 into the amo1 'high amylose Glacier'. The wild type, amo1, and sex6 genotypes gave starch phenotypes consistent with previous studies. However, the amo1sex6 double mutant yielded an unexpected phenotype, a significant increase in starch content relative to the sex6 phenotype. Amylose content (as a percentage of starch) was not increased above the level observed for the sex6 mutation alone; however, on a per seed basis, grain from lines containing the amo1 mutation (amo1 mutants and amo1sex6 double mutants) synthesize significantly more amylose than the wild-type lines and sex6 mutants. The level of granule-bound starch synthase I (GBSSI) protein in starch granules is increased in lines containing the amo1 mutation (amo1 and amo1sex6). In the amo1 genotype, starch synthase I (SSI), SSIIa, starch branching enzyme IIa (SBEIIa), and SBEIIb also markedly increased in the starch granules. Genetic mapping studies indicate that the ssIIIa gene is tightly linked to the amo1 locus, and the SSIIIa protein from the amo1 mutant has a leucine to arginine residue substitution in a conserved domain. Zymogram analysis indicates that the amo1 phenotype is not a consequence of total loss of enzymatic activity although it remains possible that the amo1 phenotype is underpinned by a more subtle change. It is therefore proposed that amo1 may be a negative regulator of other genes of starch synthesis. In this study of barley starch synthesis, the interaction between mutations at the sex 6 locus and the amo 1 locus has been characterized. Four barley genotypes, the wild type, sex 6, a mo 1, and the amo 1 sex 6 double mutant, were generated by backcrossing the sex 6 mutation present in Himalaya292 into the amo 1 ‘high amylose Glacier’. The wild type, amo 1, and sex 6 genotypes gave starch phenotypes consistent with previous studies. However, the amo 1 sex 6 double mutant yielded an unexpected phenotype, a significant increase in starch content relative to the sex 6 phenotype. Amylose content (as a percentage of starch) was not increased above the level observed for the sex 6 mutation alone; however, on a per seed basis, grain from lines containing the amo 1 mutation ( amo 1 mutants and amo 1 sex 6 double mutants) synthesize significantly more amylose than the wild-type lines and sex 6 mutants. The level of granule-bound starch synthase I (GBSSI) protein in starch granules is increased in lines containing the amo 1 mutation ( amo 1 and amo 1 sex 6). In the amo 1 genotype, starch synthase I (SSI), SSIIa, starch branching enzyme IIa (SBEIIa), and SBEIIb also markedly increased in the starch granules. Genetic mapping studies indicate that the ssIIIa gene is tightly linked to the amo 1 locus, and the SSIIIa protein from the amo 1 mutant has a leucine to arginine residue substitution in a conserved domain. Zymogram analysis indicates that the amo 1 phenotype is not a consequence of total loss of enzymatic activity although it remains possible that the amo 1 phenotype is underpinned by a more subtle change. It is therefore proposed that amo 1 may be a negative regulator of other genes of starch synthesis. |
Author | Jobling, Stephen A. Du, Xihua Jenkins, Colin L. D. Morell, Matthew K. Li, Dehong Wang, Hong Larroque, Oscar Li, Zhongyi |
AuthorAffiliation | 1 CSIRO Food Future National Research Flagship, GPO Box 1600, Canberra ACT 2601 Australia 2 CSIRO Division of Plant Industry, GPO Box 1600, Canberra, ACT 2601, Australia |
AuthorAffiliation_xml | – name: 1 CSIRO Food Future National Research Flagship, GPO Box 1600, Canberra ACT 2601 Australia – name: 2 CSIRO Division of Plant Industry, GPO Box 1600, Canberra, ACT 2601, Australia |
Author_xml | – sequence: 1 givenname: Zhongyi surname: Li fullname: Li, Zhongyi – sequence: 2 givenname: Dehong surname: Li fullname: Li, Dehong – sequence: 3 givenname: Xihua surname: Du fullname: Du, Xihua – sequence: 4 givenname: Hong surname: Wang fullname: Wang, Hong – sequence: 5 givenname: Oscar surname: Larroque fullname: Larroque, Oscar – sequence: 6 givenname: Colin L. D. surname: Jenkins fullname: Jenkins, Colin L. D. – sequence: 7 givenname: Stephen A. surname: Jobling fullname: Jobling, Stephen A. – sequence: 8 givenname: Matthew K. surname: Morell fullname: Morell, Matthew K. |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/21813797$$D View this record in MEDLINE/PubMed |
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Snippet | In this study of barley starch synthesis, the interaction between mutations at the sex6 locus and the amo1 locus has been characterized. Four barley genotypes,... In this study of barley starch synthesis, the interaction between mutations at the sex 6 locus and the amo 1 locus has been characterized. Four barley... |
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SubjectTerms | Amylose - biosynthesis Barley DNA Down-Regulation Endosperm Gene Expression Regulation, Plant Genetic loci Genetic mutation Genomics Genotypes Glaciers Grains Hordeum - enzymology Hordeum - genetics Hordeum vulgare Mutation Phenotype Plant Proteins - genetics Plant Proteins - metabolism RESEARCH PAPER Research Papers Starch - biosynthesis Starch Synthase - genetics Starch Synthase - metabolism Starches |
Title | The barley amo1 locus is tightly linked to the starch synthase IIIa gene and negatively regulates expression of granule-bound starch synthetic genes |
URI | https://www.jstor.org/stable/24040010 https://www.ncbi.nlm.nih.gov/pubmed/21813797 https://search.proquest.com/docview/1017962734 https://search.proquest.com/docview/898839426 https://pubmed.ncbi.nlm.nih.gov/PMC3193023 |
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