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Conservation and divergence of Starch Synthase III genes of monocots and dicots

Starch Synthase (SS) plays an important role in extending the α-1,4 glucan chains during starch biosynthesis by catalyzing the transfer of the glucosyl moiety from ADP-glucose to the non-reducing end of a pre-existing glucan chain. SS has five distinct isoforms of which SSIII is involved in the form...

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Autores principales: Mishra, Bhavya Priyadarshini, Kumar, Rajeev, Mohan, Amita, Gill, Kulvinder S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5730167/
https://www.ncbi.nlm.nih.gov/pubmed/29240782
http://dx.doi.org/10.1371/journal.pone.0189303
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author Mishra, Bhavya Priyadarshini
Kumar, Rajeev
Mohan, Amita
Gill, Kulvinder S.
author_facet Mishra, Bhavya Priyadarshini
Kumar, Rajeev
Mohan, Amita
Gill, Kulvinder S.
author_sort Mishra, Bhavya Priyadarshini
collection PubMed
description Starch Synthase (SS) plays an important role in extending the α-1,4 glucan chains during starch biosynthesis by catalyzing the transfer of the glucosyl moiety from ADP-glucose to the non-reducing end of a pre-existing glucan chain. SS has five distinct isoforms of which SSIII is involved in the formation of longer glucan chain length. Here we report identification and detailed characterization of ‘true’ orthologs of the well-characterized maize SSIII (ZmSSIII), among six monocots and two dicot species. ZmSSIII orthologs have nucleotide sequence similarity ranging from 56–81%. Variation in gene size among various orthologs ranged from 5.49 kb in Arabidopsis to 11.62 kb in Brachypodium and the variation was mainly due to intron size and indels present in the exons 1 and 3. Number of exons and introns were highly conserved among all orthologs however. While the intron number was conserved, intron phase showed variation at group, genera and species level except for intron 1 and 5. Several species, genera, and class specific cis-acting regulatory elements were identified in the promoter region. The predicted protein size of the SSIII orthologs ranged from 1094 amino acid (aa) in Arabidopsis to 1688 aa in Brachypodium with sequence identity ranging from 60%-89%. The N-terminal region of the protein was highly variable whereas the C-terminal region containing the Glycosyltransferase domain was conserved with >80% sequence similarity among the orthologs. In addition to confirming the known motifs, eleven novel motifs possibly providing species, genera and group specific functions, were identified in the three carbohydrate binding domains. Despite of significant sequence variation among orthologs, most of the motifs and their relative distances are highly conserved among the orthologs. The 3-D structure of catalytic region of SSIII orthologs superimposed with higher confidence confirming the presence of similar binding sites with five unidentified conserved regions in the catalytic (glycosyltransferase) domain including the pockets involved in catalysis and binding of ligands. Homeologs of wheat SSIII gene showed tissue and developmental stage specific expression pattern with the highest expression recorded in developing grains.
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spelling pubmed-57301672017-12-22 Conservation and divergence of Starch Synthase III genes of monocots and dicots Mishra, Bhavya Priyadarshini Kumar, Rajeev Mohan, Amita Gill, Kulvinder S. PLoS One Research Article Starch Synthase (SS) plays an important role in extending the α-1,4 glucan chains during starch biosynthesis by catalyzing the transfer of the glucosyl moiety from ADP-glucose to the non-reducing end of a pre-existing glucan chain. SS has five distinct isoforms of which SSIII is involved in the formation of longer glucan chain length. Here we report identification and detailed characterization of ‘true’ orthologs of the well-characterized maize SSIII (ZmSSIII), among six monocots and two dicot species. ZmSSIII orthologs have nucleotide sequence similarity ranging from 56–81%. Variation in gene size among various orthologs ranged from 5.49 kb in Arabidopsis to 11.62 kb in Brachypodium and the variation was mainly due to intron size and indels present in the exons 1 and 3. Number of exons and introns were highly conserved among all orthologs however. While the intron number was conserved, intron phase showed variation at group, genera and species level except for intron 1 and 5. Several species, genera, and class specific cis-acting regulatory elements were identified in the promoter region. The predicted protein size of the SSIII orthologs ranged from 1094 amino acid (aa) in Arabidopsis to 1688 aa in Brachypodium with sequence identity ranging from 60%-89%. The N-terminal region of the protein was highly variable whereas the C-terminal region containing the Glycosyltransferase domain was conserved with >80% sequence similarity among the orthologs. In addition to confirming the known motifs, eleven novel motifs possibly providing species, genera and group specific functions, were identified in the three carbohydrate binding domains. Despite of significant sequence variation among orthologs, most of the motifs and their relative distances are highly conserved among the orthologs. The 3-D structure of catalytic region of SSIII orthologs superimposed with higher confidence confirming the presence of similar binding sites with five unidentified conserved regions in the catalytic (glycosyltransferase) domain including the pockets involved in catalysis and binding of ligands. Homeologs of wheat SSIII gene showed tissue and developmental stage specific expression pattern with the highest expression recorded in developing grains. Public Library of Science 2017-12-14 /pmc/articles/PMC5730167/ /pubmed/29240782 http://dx.doi.org/10.1371/journal.pone.0189303 Text en © 2017 Mishra et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Mishra, Bhavya Priyadarshini
Kumar, Rajeev
Mohan, Amita
Gill, Kulvinder S.
Conservation and divergence of Starch Synthase III genes of monocots and dicots
title Conservation and divergence of Starch Synthase III genes of monocots and dicots
title_full Conservation and divergence of Starch Synthase III genes of monocots and dicots
title_fullStr Conservation and divergence of Starch Synthase III genes of monocots and dicots
title_full_unstemmed Conservation and divergence of Starch Synthase III genes of monocots and dicots
title_short Conservation and divergence of Starch Synthase III genes of monocots and dicots
title_sort conservation and divergence of starch synthase iii genes of monocots and dicots
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5730167/
https://www.ncbi.nlm.nih.gov/pubmed/29240782
http://dx.doi.org/10.1371/journal.pone.0189303
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