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作 者:Qian Tang Duorong Xu Benjamin Lenzen Andreas Brachmann Madhura MYapa Paymon Doroodian Christian Schmitz-Linneweber Tatsuru Masuda Zhihua Hua Dario Leister Tatjana Kleine
机构地区:[1]Plant Molecular Biology(Botany),Faculty of Biology,Ludwig-Maximilians-University München,82152 Martinsried,Germany [2]Molecular Genetics,Humboldt-University Berlin,Philippstr.13,10115 Berlin,Germany [3]Biocenter of the LMU Munich,Genetics Section,Grosshaderner Str.2-4,82152 Planegg-Martinsried,Germany [4]Department of Environmental and Plant Biology,Ohio University,Athens,OH 45701,USA [5]Graduate School of Arts and Sciences,The University of Tokyo,Komaba,Meguro-ku 153-8902,Tokyo,Japan
出 处:《Plant Communications》2024年第12期73-90,共18页植物通讯(英文)
基 金:Deutsche Forschungsgemeinschaft to C.S.-L.,D.L.,and T.K.(TRR175,projects A02,C01,and C05);Research in the Hua laboratory was supported by a US NSF CAREER award(MCB-1750361).
摘 要:Plastid biogenesis and the coordination of plastid and nuclear genome expression through anterograde and retrograde signaling are essential for plant development.GENOMES UNCOUPLED1(GUN1)plays a central role in retrograde signaling during early plant development.The putative function of GUN1 has been extensively studied,but its molecular function remains controversial.Here,we evaluate published transcriptome data and generate our own data from gun1 mutants grown under signaling-relevant condi-tions to show that editing and splicing are not relevant for GUN1-dependent retrograde signaling.Our study of the plastid(post)transcriptome of gun1 seedlings with white and pale cotyledons demonstrates that GUN1 deficiency significantly alters the entire plastid transcriptome.By combining this result with a penta-tricopeptide repeat code-based prediction and experimental validation by RNA immunoprecipitation ex-periments,we identified several putative targets of GUN1,including tRNAs and RNAs derived from ycf1.2,rpoC1,and rpoC2 and the ndhH–ndhA–ndhI–ndhG–ndhE–psaC–ndhD gene cluster.The absence of plastid rRNAs and the significant reduction of almost all plastid transcripts in white gun1 mutants ac-count for the cotyledon phenotype.Our study provides evidence for RNA binding and maturation as the long-sought molecular function of GUN1 and resolves long-standing controversies.We anticipate that ourfindings will serve as a basis for subsequent studies on mechanisms of plastid gene expression and will help to elucidate the function of GUN1 in retrograde signaling.
关 键 词:GUN1 MORF2 plastid(post)transcriptome retrograde signaling RIP-seq RNA binding protein
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