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马鹿MORF4L2组织表达、基因克隆及生物信息学分析
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作者 韩青 高仰 +3 位作者 吴玄烨 索婧媛 金庆梅 刘学东 《野生动物学报》 北大核心 2024年第4期774-780,共7页
MORF4L2是一种转录因子,通过形成NuA4组蛋白乙酰转移酶复合物来参与异染色质组装和组蛋白修饰,对细胞生长、增殖和凋亡起重要作用。为了探究马鹿(Cervus elaphus)鹿茸中MORF4L2所发挥的功能,使用qPCR技术检测鹿茸不同组织中MORF4L2基因... MORF4L2是一种转录因子,通过形成NuA4组蛋白乙酰转移酶复合物来参与异染色质组装和组蛋白修饰,对细胞生长、增殖和凋亡起重要作用。为了探究马鹿(Cervus elaphus)鹿茸中MORF4L2所发挥的功能,使用qPCR技术检测鹿茸不同组织中MORF4L2基因的表达水平,采用PCR克隆马鹿MORF4L2基因的CDS序列,通过多物种比对MORF4L2基因mRNA序列进行相似性分析并构建系统进化树,利用生物信息学方法预测分析MORF4L2编码蛋白的结构与理化性质。结果显示:MORF4L2在马鹿鹿茸的前软骨层中表达量最高;马鹿MORF4L2的mRNA序列较为保守,与加拿大马鹿(C.canadensis)中MORF4L2的相似性最高;马鹿MORF4L2基因CDS区全长为864 bp,编码287个氨基酸,理论等电点为9.73,为碱性蛋白;预测发现马鹿MORF4L2蛋白不存在信号肽,有30个潜在磷酸化位点;蛋白质结构主要由无规则卷曲和α-螺旋构成,主要定位在细胞核中。研究结果可为MORF4L2在马鹿鹿茸生长发育过程中所起的作用提供重要基础数据。 展开更多
关键词 马鹿 MORF4L2 组织表达 基因克隆 生物信息学
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GENOMES UNCOUPLED PROTEIN1 binds to plastid RNAs and promotes their maturation
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作者 Qian Tang Duorong Xu +8 位作者 Benjamin Lenzen Andreas Brachmann Madhura MYapa Paymon Doroodian Christian Schmitz-Linneweber Tatsuru Masuda Zhihua Hua Dario Leister Tatjana Kleine 《Plant Communications》 CSCD 2024年第12期73-90,共18页
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 retrogr... 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. 展开更多
关键词 GUN1 morf2 plastid(post)transcriptome retrograde signaling RIP-seq RNA binding protein
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