Abstract

NAC (NAM, ATAF1/2, and CUC2) proteins play a pivotal role in modulating plant development and offer protection against biotic and abiotic stresses. Until now, no systematic knowledge of NAC family genes is available for the food security crop, sweet potato. Here, a comprehensive genome-wide survey of NAC domain-containing proteins identified 130 ItbNAC and 144 ItfNAC genes with full length sequences in the genomes of two diploid wild relatives of cultivated sweet potato, Ipomoea triloba and Ipomoea trifida, respectively. These genes were physically mapped onto 15 I. triloba and 16 I. trifida chromosomes, respectively. Phylogenetic analysis divided all 274 NAC proteins into 20 subgroups together with NAC transcription factors (TFs) from Arabidopsis. There were 9 and 15 tandem duplication events in the I. triloba and I. trifida genomes, respectively, indicating an important role of tandem duplication in sweet potato gene expansion and evolution. Moreover, synteny analysis suggested that most NAC genes in the two diploid sweet potato species had a similar origin and evolutionary process. Gene expression patterns based on RNA-Seq data in different tissues and in response to various hormone, biotic or abiotic treatments revealed their possible involvement in organ development and response to various biotic/abiotic stresses. The expression of 36 NAC TFs, which were upregulated in the five tissues and in response to mannitol treatment, was also determined by real-time quantitative polymerase chain reaction (RT-qPCR) in hexaploid cultivated sweet potato exposed to drought stress. Those results largely corroborated the expression profile of mannitol treatment uncovered by the RNA-Seq data. Some significantly up-regulated genes related to drought stress, such as ItbNAC110, ItbNAC114, ItfNAC15, ItfNAC28, and especially ItfNAC62, which had a conservative spatial conformation with a closely related paralogous gene, ANAC019, may be potential candidate genes for a sweet potato drought tolerance breeding program. This analysis provides comprehensive and systematic information about NAC family genes in two diploid wild relatives of cultivated sweet potato, and will provide a blueprint for their functional characterization and exploitation to improve the tolerance of sweet potato to abiotic stresses.

Highlights

  • No apical meristem (NAM), ATAF1/2, and CUC2 (NAC) transcription factor (TF) family genes, which serve as molecular switches in the temporal and spatial regulation of the expression of their target genes, are an abundant group of plant-specific proteins

  • We retrieved a total of 283 non-redundant NAC domain-containing TFs from the I. triloba and I. trifida genomes by local BLASTP and HMMER searches, and these 283 sweet potato NAC TFs were renamed as ItbNAC1 to ItbNAC132, and ItfNAC1 to ItfNAC151 based on their chromosomal localization in I. triloba and I. trifida genomes, respectively

  • Most of the identified NAC proteins were localized in the nucleus, i.e., 98 ItbNACs and 109 ItfNACs, followed by 20 ItbNACs and 19 ItfNACs that were localized in the cytoplasm

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Summary

Introduction

NAM, ATAF1/2, and CUC2 (NAC) transcription factor (TF) family genes, which serve as molecular switches in the temporal and spatial regulation of the expression of their target genes, are an abundant group of plant-specific proteins. NAC TFs are derived from three superfamilies: No apical meristem (NAM), Arabidopsis transcription activation factor (ATAF), and Cupshaped cotyledon (CUC) (Souer et al, 1996; Puranik et al, 2012). In Arabidopsis thaliana, the NAC domain TF NAC016 binds directly to the promoter of ABSCISIC ACID-RESPONSIVE ELEMENT BINDING PROTEIN1 (AREB1) and negatively regulates plant drought tolerance (Sakuraba et al, 2015), while over-expression of either of three homologous genes, ANAC019, ANAC072 or ANAC055, in A. thaliana conferred significantly fortified drought resistance (Tran et al, 2004). Drought tolerance-related NAC genes were reported in tomato (Solanum lycopersicum), such as the NAC factor JUNGBRUNNEN1 (SlJUB1), which positively regulated drought tolerance by controlling the expression of three TFs, SlDREB1, SlDREB2 and SlDELLA (Thirumalaikumar et al, 2018)

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