4.7 Article

Comparative proteomic analysis of chromosome segment substitution lines of Thai jasmine rice KDML105 under short-term salinity stress

Journal

PLANTA
Volume 256, Issue 1, Pages -

Publisher

SPRINGER
DOI: 10.1007/s00425-022-03929-9

Keywords

Rice (Oryza sativa L; ); Salinity stress; Salinity tolerance; Rice proteomics; Chromosome segment substitution line (CSSL); Thai jasmine rice; Climate change

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Funding

  1. Kasetsart University
  2. Kasetsart University Research and Development Institute (KURDI), Bangkok, Thailand

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In this study, the proteomic profiles of chromosome segment substitution lines (CSSLs) developed from a Thai jasmine rice cultivar under salinity stress were investigated. The results showed that various proteins involved in DNA replication and transcription, stress and defense, protein transport and trafficking, carbohydrate metabolic process, signal transduction, and cell structure were up-regulated in CSSLs under salinity stress. The protein interaction network analysis revealed connections between proteins involved in cell wall synthesis, transcription, translation, and defense responses.
Main conclusions Heat shock proteins, ROS detoxifying enzymes, and ion homeostasis proteins, together with proteins in carbohydrate metabolism, cell structure, brassinosteroids, and carotenoid biosynthesis pathway were up-regulated in CSSLs under salinity stress. Rice is one of the most consumed staple foods worldwide. Salinity stress is a serious global problem affecting rice productivity. Many attempts have been made to select or produce salinity-tolerant rice varieties. Genetics and biochemical approaches were used to study the salinity-responsive pathway in rice to develop salinity tolerant strains. This study investigated the proteomic profiles of chromosome segment substitution lines (CSSLs) developed from KDML105 (Khao Dawk Mali 105, a Thai jasmine rice cultivar) under salinity stress. The CSSLs showed a clear resistant phenotype in response to 150 mM NaCl treatment compared to the salinity-sensitive line, IR29. Liquid chromatography-tandem mass spectrometry using the Ultimate 3000 Nano/Capillary LC System coupled to a Hybrid Quadrupole Q-Tof Impact II (TM) equipped with a nano-captive spray ion source was applied for proteomic analysis. Based on our criteria, 178 proteins were identified as differentially expressed proteins under salinity stress. Protein functions in DNA replication and transcription, and stress and defense accounted for the highest proportions in response to salinity stress, followed by protein transport and trafficking, carbohydrate metabolic process, signal transduction, and cell structure. The protein interaction network among the 75 up-regulated proteins showed connections between proteins involved in cell wall synthesis, transcription, translation, and in defense responses.

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