Abstract

Secondary wall-associated NAC (SWN) genes are a subgroup of NAC (NAM, ATAF, and CUC) transcription factors (TF) that play a key role in regulating secondary cell wall biosynthesis in plants. However, this gene family has not been systematically characterized, and their potential roles in response to hormones are unknown in Nicotiana tabacum. In this study, a total of 40 SWN genes, of which 12 from Nicotiana tomentosiformis, 13 from Nicotiana sylvestris, and 15 from Nicotiana tabacum, were successfully identified. The 15 SWNs from Nicotiana tabacum were further classified into three groups, namely, vascular-related NAC domain genes (NtVNDs), NAC secondary wall thickening promoting factor genes (NtNSTs), and secondary wall-associated NAC domain genes (NtSNDs). The protein characteristic, gene structure, and chromosomal location of 15 NtSWNs (also named Nt1 to Nt15) were also analyzed. The NtVND and NtNST group genes had five conserved subdomains in their N-terminal regions and a motif (LP[Q/x] L[E/x] S[P/A]) in their diverged C- terminal regions. Some hormones, dark and low-temperature related cis-acting elements, were significantly enriched in the promoters of NtSWN genes. A comprehensive expression profile analysis revealed that Nt4 and Nt12 might play a role in vein development. Others might be important for stem development. Quantitative reverse transcription-polymerase chain reaction (qRT-PCR) revealed that in the NtNST group, genes such as Nt7, Nt8, and Nt13 were more sensitive than the genes in NtVND and NtSND groups under abiotic stress conditions. A transactivation assay further suggested that Nt7, Nt8, and Nt13 showed a significant transactivation activity. Overall, SWN genes were finally identified and characterized in diploid and tetraploid tobacco, revealing new insights into their evolution, variation, and homology relationships. Transcriptome, cis-acting element, qRT-PCR, and transactivation assay analysis indicated the roles in hormonal and stress responses, which provided further resources in molecular mechanism and genetic improvement.

Highlights

  • Secondary cell walls are mainly made up of xylem treachery elements and fibers (Zhong and Ye, 2015a), which are present in the plant cells but absent in the animal cells

  • A two-hybrid assay of yeast revealed the ability of AtVND7 to form homodimers and heterodimers with other AtVND proteins (Yamaguchi et al, 2008). These results indicate that secondary wall biosynthesis is a complex and delicate process; AtSWN protein sequences (AtSWNs) genes from the NAC family are key transcription factor (TF)

  • We identified a total of 40 secondary-wall associated NAC transcriptional factors from Nicotiana tabacum (K326), Nicotiana sylvestris, and Nicotiana tomentosiformis

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Summary

Introduction

Secondary cell walls are mainly made up of xylem treachery elements and fibers (Zhong and Ye, 2015a), which are present in the plant cells but absent in the animal cells. They can protect plant cells from potential biotic and abiotic stresses (Brown et al, 2005). After a comparative genome analysis across 19 higher plant species, SWN transcriptional factors, including three groups, SND, NST, and VND, were identified as playing a crucial and ruling role in secondary cell wall biosynthesis (Yao et al, 2012)

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