Kimoto R: The anaerobic proteins of maize. Cell 1980, 20:761-767. 5. Sachs MM > 자유게시판

Kimoto R: The anaerobic proteins of maize. Cell 1980, 20:761-767. 5. S…

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Kimoto R: The anaerobic proteins of maize. Mobile 1980, 20:761-767. 5. Sachs MM, Subbaiah CC, Saab IN: Anaerobic gene expression and flooding tolerance in maize. J Exp Bot 1996, forty seven:1-15. six. Chang WWP, Huang L, Shen M, Webster C, Burlingame AL, Roberts JKM: Patterns of protein synthesis and tolerance of anoxia in root strategies of maize seedlings acclimated to the low-oxygen surroundings, and identification of proteins by mass spectrometry. Plant Physiol 2000, 122:295-318. seven. Klok EJ, Wilson IW, Wilson D, Chapman SC, Ewing RM, omerville SC, Peacock WJ, Dolferus R, Dennis ES: Expression profile examination in the lowoxygen response in Arabidopsis root cultures. Plant Cell 2002, 14:2481-2494. 8. Tsuji H, Nakazono M, Saisho D, Tsutsumi N, Hirai A: Transcript levels of the nuclear-encoded respiratory genes in rice reduce by oxygen deprivation: evidence for involvement of calcium in expression on the different oxidase 1a gene. FEBS Lett 2000, 471:201-204. nine. Baxter-Burrell A, Chang R, Springer PS, Bailey-Serres J: Gene and enhancer entice transposable features reveal oxygen deprivation-regulated genes and 1,3-Dimethoxybenzene their advanced patterns of expression in Arabidopsis. Ann Bot 2003, 91:129-141. 10. Baxter-Burrell A, Yang Z, Springer PS, Bailey-Serres J: ROPGAP4-dependent Rop GTPase rheostat controls of Arabidopsis oxygen PubMed ID: deprivation tolerance. Science 2002, 296:2026-2028. eleven. Snedden WA, Fromm H: Calmodulin as being a flexible calcium sign transducer in vegetation. New Phytol 2001, 151:35-66.Conclusion To get an perception into how the roots of maize seedlings respond to waterlogging on the late stage, we completed gene expression profiling at 4 time details (12 h, sixteen h, 20 h, and 24 h) after waterlogging cure using tolerant inbred line HZ32. Annotation and evaluation depending on gene ontology conditions instructed that waterlogging affected a broad spectrum of practical types. For the late stage of waterlogging, amino acid metabolic process performs an important role linked to protein degradation and carbon fat burning capacity. It can be believed being involved in regulation of cytoplasmic pH and breakdown of carbon skeletons with the provide of vitality. Signal transduction is still energetic and it is distinct from all those signaling pathways induced in early levels, perhaps due to the will need to regulate the tolerance system for survival beneath prolonged waterlogging. We propose the reaction to waterlogging ought to be conceptually divided into two stages: protection and adaption. The new genes connected to sign transduction identified in this review could execute crucial roles in regulating the reaction to waterlogging for the late phase and supply new insights to the reaction to waterlogging in maize. A complete of 63 candidate genes for waterlogging tolerance were validated by in silico mapping by way of a candidate gene approach. These genes could possibly be crucial candidates for more breeding of waterlogging-tolerant crops, but will require even further verification. The identification of unique genes influencing intricate qualities is usually one particular of your most tough duties in genetics. By researching which genes are induced on the late phase in response to waterlogging in the roots of maize seedlings, we've got presented the idea for even more investigation in this particular subject. Sense/antisense over-expression ofZou et al. BMC Plant Biology 2010, ten:189 15 of12. Subbaiah CC, Sachs MM: Maize cap1 encodes a novel SERCA-type calcium ATPase with a calmodulin-binding area. J Biol C.


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