Genome‐Wide Identification of Pentatricopeptide Repeat (PPR) Gene Family and Multi‐Omics Analysis Provide New Insights Into the Albinism Mechanism of Kandelia obovata Propagule Leaves

Author:

Xu Chaoqun1,Wang Ji‐Cheng1,Sun Ling1,Zhuang Li‐Han1,Guo Ze‐Jun12,Ding Qian‐Su1,Ma Dong‐Na13,Song Ling‐Yu1,Li Jing1,Tang Han‐Chen1,Zhu Xue‐Yi1ORCID,Zheng Hai‐Lei1ORCID

Affiliation:

1. Key Laboratory of the Ministry of Education for Coastal and Wetland Ecosystems, College of the Environment and Ecology Xiamen University Xiamen China

2. Guangxi Laboratory on the Study of Coral Reefs in the South China Sea, School of Marine Sciences, Coral Reef Research Center of China Guangxi University Nanning China

3. National Engineering Research Center of Cereal Fermentation and Food Biomanufacturing, School of Food Science and Technology Jiangnan University Wuxi Jiangsu China

Abstract

ABSTRACTPentatricopeptide repeat (PPR) gene family constitutes one of the largest gene families in plants, which mainly participate in RNA editing and RNA splicing of organellar RNAs, thereby affecting the organellar development. Recently, some evidence elucidated the important roles of PPR proteins in the albino process of plant leaves. However, the functions of PPR genes in the woody mangrove species have not been investigated. In this study, using a typical true mangrove Kandelia obovata, we systematically identified 298 PPR genes and characterized their general features and physicochemical properties, including evolutionary relationships, the subcellular localization, PPR motif type, the number of introns and PPR motifs, and isoelectric point, and so forth. Furthermore, we combined genome‐wide association studies (GWAS) and transcriptome analysis to identify the genetic architecture and potential PPR genes associated with propagule leaves colour variations of K. obovata. As a result, we prioritized 16 PPR genes related to the albino phenotype using different strategies, including differentially expressed genes analysis and genetic diversity analysis. Further analysis discovered two genes of interest, namely Maker00002998 (PLS‐type) and Maker00003187 (P‐type), which were differentially expressed genes and causal genes detected by GWAS analysis. Moreover, we successfully predicted downstream target chloroplast genes (rps14, rpoC1 and rpoC2) bound by Maker00002998 PPR proteins. The experimental verification of RNA editing sites of rps14, rpoC1, and rpoC2 in our previous study and the verification of interaction between Maker00002998 and rps14 transcript using in vitro RNA pull‐down assays revealed that Maker00002998 PPR protein might be involved in the post‐transcriptional process of chloroplast genes. Our result provides new insights into the roles of PPR genes in the albinism mechanism of K. obovata propagule leaves.

Publisher

Wiley

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