BrPARP1, a Poly (ADP-Ribose) Polymerase Gene, Is Involved in Root Development in Brassica rapa under Drought Stress

• Published in: Horticulturae Vol. 8; no. 1; p. 78
• Main Authors: Cao, Gangqiang, Jiang, Wenjing, Shi, Gongyao, Tian, Zhaoran, Shang, Jingjing, Xie, Zhengqing, Chen, Weiwei, Tian, Baoming, Wei, Xiaochun, Wei, Fang, Gu, Huihui
• Format: Journal Article
• Language: English
• Published: Basel MDPI AG 01.01.2022
• Subjects: Abiotic stress; Adenosine diphosphate; Apoptosis; Bioinformatics; Biological activity; Brassica; Cell division; DNA damage; Drought; Energy consumption; Enzymatic activity; Enzyme activity; Enzymes; Gene expression; Genes; Genomes; Homology; Malondialdehyde; Mutation; NAD; Pattern analysis; Physiology; Plant growth; Plant roots; Poly(ADP-ribose) polymerase; Poly(ADP-ribose) Polymerase 1; Polymers; Proline; Proteins; Reactive oxygen species; Ribose; Ribozymes; RNA-mediated interference; Root development; root growth; Scavenging; Substrates; Transgenic plants; whole-genome triplication
• DOI: 10.3390/horticulturae8010078
• ISSN: 2311-7524

PARP proteins are highly conserved homologs among the eukaryotic poly (ADP-ribose) polymerases. After activation, ADP-ribose polymers are synthesized on a series of ribozymes that use NAD+ as a substrate. PARPs participate in the regulation of various important biological processes, such as plant growth, development, and stress response. In this study, we characterized the homologue of PARP1 in B. rapa using RNA interference (RNAi) to reveal the underlying mechanism responding to drought stress. Bioinformatics and expression pattern analyses demonstrated that two copy numbers of PARP1 genes (BrPARP1.A03 and BrPARP1.A05) in B. rapa following a whole-genome triplication (WGT) event were retained compared with Arabidopsis, but only BrPARP1.A03 was predominantly transcribed in plant roots. Silencing of BrPARP1 could markedly promote root growth and development, probably via regulating cell division, and the transgenic Brassica lines showed more tolerance under drought treatment, accompanied with substantial alterations including accumulated proline contents, significantly reduced malondialdehyde, and increased antioxidative enzyme activity. In addition, the findings showed that the expression of stress-responsive genes, as well as reactive oxygen species (ROS)-scavenging related genes, was largely reinforced in the transgenic lines under drought stress. In general, these results indicated that BrPARP1 likely responds to drought stress by regulating root growth and the expression of stress-related genes to cope with adverse conditions in B. rapa.