Cargando…

Wheat NAM genes regulate the majority of early monocarpic senescence transcriptional changes including nitrogen remobilization genes

Senescence enables the remobilization of nitrogen and micronutrients from vegetative tissues of wheat (Triticum aestivum L.) into the grain. Understanding the molecular players in this process will enable the breeding of wheat lines with tailored grain nutrient content. The NAC transcription factor...

Descripción completa

Detalles Bibliográficos
Autores principales: Andleeb, Tayyaba, Knight, Emilie, Borrill, Philippa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9911049/
https://www.ncbi.nlm.nih.gov/pubmed/36226803
http://dx.doi.org/10.1093/g3journal/jkac275
_version_ 1784884918028861440
author Andleeb, Tayyaba
Knight, Emilie
Borrill, Philippa
author_facet Andleeb, Tayyaba
Knight, Emilie
Borrill, Philippa
author_sort Andleeb, Tayyaba
collection PubMed
description Senescence enables the remobilization of nitrogen and micronutrients from vegetative tissues of wheat (Triticum aestivum L.) into the grain. Understanding the molecular players in this process will enable the breeding of wheat lines with tailored grain nutrient content. The NAC transcription factor NAM-B1 is associated with earlier senescence and higher levels of grain protein, iron, and zinc contents due to increased nutrient remobilization. To investigate how related NAM genes control nitrogen remobilization at the molecular level, we carried out a comparative transcriptomic study using flag leaves at 7 time points (3, 7, 10, 13, 15, 19, and 26 days after anthesis) in wild type and NAM RNA interference lines with reduced NAM gene expression. Approximately 2.5 times more genes were differentially expressed in wild type than NAM RNA interference plants during this early senescence time course (6,508 vs 2,605 genes). In both genotypes, differentially expressed genes were enriched for gene ontology terms related to photosynthesis, hormones, amino acid transport, and nitrogen metabolism. However, nitrogen metabolism genes including glutamine synthetase (GS1 and GS2), glutamate decarboxylase (GAD), glutamate dehydrogenase (GDH), and asparagine synthetase (ASN1) showed stronger or earlier differential expression in wild-type than in NAM RNA interference plants, consistent with higher nitrogen remobilization. The use of time course data identified the dynamics of NAM-regulated and NAM-independent gene expression changes during senescence and provides an entry point to functionally characterize the pathways regulating senescence and nutrient remobilization in wheat.
format Online
Article
Text
id pubmed-9911049
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-99110492023-02-13 Wheat NAM genes regulate the majority of early monocarpic senescence transcriptional changes including nitrogen remobilization genes Andleeb, Tayyaba Knight, Emilie Borrill, Philippa G3 (Bethesda) Plant Genetics and Genomics Senescence enables the remobilization of nitrogen and micronutrients from vegetative tissues of wheat (Triticum aestivum L.) into the grain. Understanding the molecular players in this process will enable the breeding of wheat lines with tailored grain nutrient content. The NAC transcription factor NAM-B1 is associated with earlier senescence and higher levels of grain protein, iron, and zinc contents due to increased nutrient remobilization. To investigate how related NAM genes control nitrogen remobilization at the molecular level, we carried out a comparative transcriptomic study using flag leaves at 7 time points (3, 7, 10, 13, 15, 19, and 26 days after anthesis) in wild type and NAM RNA interference lines with reduced NAM gene expression. Approximately 2.5 times more genes were differentially expressed in wild type than NAM RNA interference plants during this early senescence time course (6,508 vs 2,605 genes). In both genotypes, differentially expressed genes were enriched for gene ontology terms related to photosynthesis, hormones, amino acid transport, and nitrogen metabolism. However, nitrogen metabolism genes including glutamine synthetase (GS1 and GS2), glutamate decarboxylase (GAD), glutamate dehydrogenase (GDH), and asparagine synthetase (ASN1) showed stronger or earlier differential expression in wild-type than in NAM RNA interference plants, consistent with higher nitrogen remobilization. The use of time course data identified the dynamics of NAM-regulated and NAM-independent gene expression changes during senescence and provides an entry point to functionally characterize the pathways regulating senescence and nutrient remobilization in wheat. Oxford University Press 2022-10-13 /pmc/articles/PMC9911049/ /pubmed/36226803 http://dx.doi.org/10.1093/g3journal/jkac275 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of Genetics Society of America. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Plant Genetics and Genomics
Andleeb, Tayyaba
Knight, Emilie
Borrill, Philippa
Wheat NAM genes regulate the majority of early monocarpic senescence transcriptional changes including nitrogen remobilization genes
title Wheat NAM genes regulate the majority of early monocarpic senescence transcriptional changes including nitrogen remobilization genes
title_full Wheat NAM genes regulate the majority of early monocarpic senescence transcriptional changes including nitrogen remobilization genes
title_fullStr Wheat NAM genes regulate the majority of early monocarpic senescence transcriptional changes including nitrogen remobilization genes
title_full_unstemmed Wheat NAM genes regulate the majority of early monocarpic senescence transcriptional changes including nitrogen remobilization genes
title_short Wheat NAM genes regulate the majority of early monocarpic senescence transcriptional changes including nitrogen remobilization genes
title_sort wheat nam genes regulate the majority of early monocarpic senescence transcriptional changes including nitrogen remobilization genes
topic Plant Genetics and Genomics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9911049/
https://www.ncbi.nlm.nih.gov/pubmed/36226803
http://dx.doi.org/10.1093/g3journal/jkac275
work_keys_str_mv AT andleebtayyaba wheatnamgenesregulatethemajorityofearlymonocarpicsenescencetranscriptionalchangesincludingnitrogenremobilizationgenes
AT knightemilie wheatnamgenesregulatethemajorityofearlymonocarpicsenescencetranscriptionalchangesincludingnitrogenremobilizationgenes
AT borrillphilippa wheatnamgenesregulatethemajorityofearlymonocarpicsenescencetranscriptionalchangesincludingnitrogenremobilizationgenes