FRINK Linked Data Fragments server

Matches in SemOpenAlex for { <https://semopenalex.org/work/W4300863169> ?p ?o ?g. }

• W4300863169 abstract "Drought stress is one of the major abiotic stress factors that affect plant growth and crop productivity. Tartary buckwheat is a nutritionally balanced and flavonoid-rich pseudocereal crop and also has strong adaptability to different adverse environments including drought. However, little is known about its drought tolerance mechanism. In this study, we performed comparative physiological and transcriptomic analyses of two contrasting drought-resistant Tartary buckwheat genotypes under nature drought treatment in the reproductive stage. Under drought stress, the drought-tolerant genotype XZSN had significantly higher contents of relative water, proline, and soluble sugar, as well as lower relative electrolyte leakage in the leaves than the drought-susceptible LK3. A total of 5,058 (2,165 upregulated and 2,893 downregulated) and 5,182 (2,358 upregulated and 2,824 downregulated) potential drought-responsive genes were identified in XZSN and LK3 by transcriptome sequencing analysis, respectively. Among the potential drought-responsive genes of XZSN, 1,206 and 1,274 genes were identified to be potential positive and negative contributors for XZSN having higher drought resistance ability than LK3. Furthermore, 851 out of 1,206 positive drought-resistant genes were further identified to be the core drought-resistant genes of XZSN based on WGCNA analysis, and most of them were induced earlier and quicker by drought stress than those in LK3. Functional annotation of the 851 core drought-resistant genes found that a large number of stress-responsive genes were involved in TFs, abscisic acid (ABA) biosynthesis, signal transduction and response, non-ABA signal molecule biosynthesis, water holding, oxygen species scavenging, osmotic adjustment, cell damage prevention, and so on. Transcriptional regulatory network analyses identified the potential regulators of these drought-resistant functional genes and found that the HD-ZIP and MYB TFs might be the key downstream TFs of drought resistance in Tartary buckwheat. Taken together, these results indicated that the XZSN genotype was more drought-tolerant than the LK3 genotype as evidenced by triggering the rapid and dramatic transcriptional reprogramming of drought-resistant genes to reduce water loss, prevent cell damage, and so on. This research expands our current understanding of the drought tolerance mechanisms of Tartary buckwheat and provides important information for its further drought resistance research and variety breeding." @default.
• W4300863169 created "2022-10-04" @default.
• W4300863169 creator A5005589952 @default.
• W4300863169 creator A5009453453 @default.
• W4300863169 creator A5014120192 @default.
• W4300863169 creator A5055730219 @default.
• W4300863169 creator A5072116470 @default.
• W4300863169 creator A5077892879 @default.
• W4300863169 creator A5086226547 @default.
• W4300863169 creator A5089998194 @default.
• W4300863169 date "2022-10-03" @default.
• W4300863169 modified "2023-10-16" @default.
• W4300863169 title "Comparative physiological, transcriptomic, and WGCNA analyses reveal the key genes and regulatory pathways associated with drought tolerance in Tartary buckwheat" @default.
• W4300863169 cites W1270834676 @default.
• W4300863169 cites W1510120983 @default.
• W4300863169 cites W1894241104 @default.
• W4300863169 cites W1963843265 @default.
• W4300863169 cites W1966327575 @default.
• W4300863169 cites W2027847170 @default.
• W4300863169 cites W2035558044 @default.
• W4300863169 cites W2036591688 @default.
• W4300863169 cites W2063794514 @default.
• W4300863169 cites W2080328685 @default.
• W4300863169 cites W2092775357 @default.
• W4300863169 cites W2119034410 @default.
• W4300863169 cites W2122056398 @default.
• W4300863169 cites W2123060905 @default.
• W4300863169 cites W2133723605 @default.
• W4300863169 cites W2134526812 @default.
• W4300863169 cites W2140729960 @default.
• W4300863169 cites W2140952049 @default.
• W4300863169 cites W2146394721 @default.
• W4300863169 cites W2157236929 @default.
• W4300863169 cites W2168740498 @default.
• W4300863169 cites W2210162831 @default.
• W4300863169 cites W2227280755 @default.
• W4300863169 cites W2280021931 @default.
• W4300863169 cites W2338823525 @default.
• W4300863169 cites W2342747650 @default.
• W4300863169 cites W2527891094 @default.
• W4300863169 cites W2530829436 @default.
• W4300863169 cites W2532983971 @default.
• W4300863169 cites W2547854432 @default.
• W4300863169 cites W2566127063 @default.
• W4300863169 cites W2606142504 @default.
• W4300863169 cites W2609642167 @default.
• W4300863169 cites W2662563668 @default.
• W4300863169 cites W2736519455 @default.
• W4300863169 cites W2738449837 @default.
• W4300863169 cites W2747055003 @default.
• W4300863169 cites W2752852083 @default.
• W4300863169 cites W2755811281 @default.
• W4300863169 cites W2810899639 @default.
• W4300863169 cites W2883356104 @default.
• W4300863169 cites W2887453170 @default.
• W4300863169 cites W2931032418 @default.
• W4300863169 cites W2943950715 @default.
• W4300863169 cites W2946357568 @default.
• W4300863169 cites W2953065537 @default.
• W4300863169 cites W2964214782 @default.
• W4300863169 cites W2972889883 @default.
• W4300863169 cites W2978415014 @default.
• W4300863169 cites W2983263940 @default.
• W4300863169 cites W2995276351 @default.
• W4300863169 cites W3004608790 @default.
• W4300863169 cites W3014666998 @default.
• W4300863169 cites W3034045599 @default.
• W4300863169 cites W3036264198 @default.
• W4300863169 cites W3043269944 @default.
• W4300863169 cites W3089071126 @default.
• W4300863169 cites W3093224024 @default.
• W4300863169 cites W3113569695 @default.
• W4300863169 cites W3119003175 @default.
• W4300863169 cites W3137300448 @default.
• W4300863169 cites W3145340763 @default.
• W4300863169 cites W3151212277 @default.
• W4300863169 cites W3157075906 @default.
• W4300863169 cites W3157679614 @default.
• W4300863169 cites W3163647467 @default.
• W4300863169 cites W3171525984 @default.
• W4300863169 cites W3175435983 @default.
• W4300863169 cites W3181344308 @default.
• W4300863169 cites W3199247631 @default.
• W4300863169 cites W4211132461 @default.
• W4300863169 cites W4214925970 @default.
• W4300863169 cites W4225878238 @default.
• W4300863169 doi "https://doi.org/10.3389/fpls.2022.985088" @default.
• W4300863169 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/36262653" @default.
• W4300863169 hasPublicationYear "2022" @default.
• W4300863169 type Work @default.
• W4300863169 citedByCount "3" @default.
• W4300863169 countsByYear W43008631692023 @default.
• W4300863169 crossrefType "journal-article" @default.
• W4300863169 hasAuthorship W4300863169A5005589952 @default.
• W4300863169 hasAuthorship W4300863169A5009453453 @default.
• W4300863169 hasAuthorship W4300863169A5014120192 @default.
• W4300863169 hasAuthorship W4300863169A5055730219 @default.
• W4300863169 hasAuthorship W4300863169A5072116470 @default.
• W4300863169 hasAuthorship W4300863169A5077892879 @default.
• W4300863169 hasAuthorship W4300863169A5086226547 @default.

• next