Isolation, Characterization, and Expression Analysis of NAC Transcription Factor from Andrographis paniculata (Burm. f.) Nees and Their Role in Andrographolide Production

Author:

Kumar Ramesh12ORCID,Kumar Chavlesh3,Roy Choudhury Debjani1,Ranjan Aashish4,Raipuria Ritesh Kumar4,Dubey Kaushik Kumar Dhar2,Mishra Ayushi5ORCID,Kumar Chetan67,Manzoor Malik Muzafar6ORCID,Kumar Ashok8,Kumari Abha2ORCID,Singh Kuldeep910,Singh Gyanendra Pratap9,Singh Rakesh1ORCID

Affiliation:

1. Division of Genomic Resources, ICAR-National Bureau of Plant Genetic Resources, New Delhi 110012, Delhi, India

2. Amity Institute of Biotechnology, Amity University, Noida 201313, Uttar Pradesh, India

3. Division of Fruits and Horticultural Technology, ICAR-Indian Agricultural Research Institute, New Delhi 110012, Delhi, India

4. National Institute of Plant Genome Research, Aruna Asaf Ali Marg, New Delhi 110067, Delhi, India

5. School of Biotechnology, Jawaharlal Nehru University, New Delhi 110067, Delhi, India

6. CSIR-Indian Institute of Integrative Medicine, Jammu 180001, Jammu and Kashmir, India

7. School of Pharmaceutical & Populations Health Informatics, DIP University Mussoorie-Dehradun, Dehradun 248009, Uttrakhand, India

8. Division of Germplasm Evaluation, ICAR-National Bureau of Plant Genetic Resources, New Delhi 110012, Delhi, India

9. ICAR-National Bureau of Plant Genetic Resources, New Delhi 110012, Delhi, India

10. International Crops Research Institute for Semi-Arid Tropics, Hyderabad 502324, Telangana, India

Abstract

Andrographis paniculata (Burm. f.) Nees is an important medicinal plant known for its bioactive compound andrographolide. NAC transcription factors (NAM, ATAF1/2, and CUC2) play a crucial role in secondary metabolite production, stress responses, and plant development through hormonal signaling. In this study, a putative partial transcript of three NAC family genes (ApNAC83, ApNAC21 22 and ApNAC02) was used to isolate full length genes using RACE. Bioinformatics analyses such as protein structure prediction, cis-acting regulatory elements, and gene ontology analysis were performed. Based on in silico predictions, the diterpenoid profiling of the plant’s leaves (five-week-old) and the real-time PCR-based expression analysis of isolated NAC genes under abscisic acid (ABA) treatment were performed. Additionally, the expression analysis of isolated NAC genes under MeJA treatment and transient expression in Nicotiana tabacum was performed. Full-length sequences of three members of the NAC transcription factor family, ApNAC83 (1102 bp), ApNAC21 22 (996 bp), and ApNAC02 (1011 bp), were isolated and subjected to the promoter and gene ontology analysis, which indicated their role in transcriptional regulation, DNA binding, ABA-activated signaling, and stress management. It was observed that ABA treatment leads to a higher accumulation of andrographolide and 14-deoxyandrographolide content, along with the upregulation of ApNAC02 (9.6-fold) and the downregulation of ApNAC83 and ApNAC21 22 in the leaves. With methyl jasmonate treatment, ApNAC21 22 expression decreased, while ApNAC02 increased (1.9-fold), with no significant change being observed in ApNAC83. The transient expression of the isolated NAC genes in a heterologous system (Nicotiana benthamiana) demonstrated their functional transcriptional activity, leading to the upregulation of the NtHMGR gene, which is related to the terpene pathway in tobacco. The expression analysis and heterologous expression of ApNAC21 22 and ApNAC02 indicated their role in andrographolide biosynthesis.

Funder

ICAR-National Bureau of Plant Genetic Resources

Publisher

MDPI AG

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