Genome-Wide Identification, Characterization, and Expression Analysis of the NAC Transcription Factor in Chenopodium quinoa
The NAC (NAM, ATAF, and CUC) family is one of the largest families of plant-specific transcription factors. It is involved in many plant growth and development processes, as well as abiotic/biotic stress responses. So far, little is known about the NAC family in . In the present study, a total of 90...
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Published in: | Genes Vol. 10; no. 7; p. 500 |
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Main Authors: | , , , , , , , , , |
Format: | Journal Article |
Language: | English |
Published: |
Switzerland
MDPI AG
30-06-2019
MDPI |
Subjects: | |
Online Access: | Get full text |
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Summary: | The NAC (NAM, ATAF, and CUC) family is one of the largest families of plant-specific transcription factors. It is involved in many plant growth and development processes, as well as abiotic/biotic stress responses. So far, little is known about the NAC family in
. In the present study, a total of 90
were identified in quinoa (named as
) and phylogenetically divided into 14 distinct subfamilies. Different subfamilies showed diversities in gene proportions, exon-intron structures, and motif compositions. In addition, 28
duplication events were investigated, and a strong subfamily preference was found during the
expansion in quinoa, indicating that the duplication event was not random across
subfamilies during quinoa evolution. Moreover, the analysis of Ka/Ks (non-synonymous substitution rate/synonymous substitution rate) ratios suggested that the duplicated
might have mainly experienced purifying selection pressure with limited functional divergence. Additionally, 11 selected
showed significant tissue-specific expression patterns, and all the
were positively regulated in response to salt stress. The result provided evidence for selecting candidate genes for further characterization in tissue/organ specificity and their functional involvement in quinoa's strong salinity tolerance. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 2073-4425 2073-4425 |
DOI: | 10.3390/genes10070500 |