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Structural and functional characterizations of mung bean mitochondrial nucleoids.

机译:绿豆线粒体核苷酸的结构和功能表征。

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Mitochondrial nucleoids isolated from mung bean seedlings exhibited a chromatin-like structure associated with a membrane component. A similar structure, which underwent discrete changes during cotyledon development, was identified in situ. Isolated nucleoids consisted of essentially the same phospholipids, including cardiolipin, as whole mitochondria and proteins of inner- and outer-mitochondrial-membrane origin. Actin was consistently found with mitochondrial nucleoids prepared with different detergent concentrations. Formaldehyde cross-linking of cytochalasin B- and proteinase K-treated mitochondria further revealed that actin was associated with DNA in nucleoids. Mitochondrial nucleoids were self-sufficient in directing DNA synthesis in vitro in a pattern mimicking mtDNA synthesis in isolated mitochondria. In pulse-field gel electrophoresis, newly synthesized mtDNA separated into two major components, well-bound and fast-moving forms. Nucleoids DNA synthesis was resistant to aphidicolin but sensitive to N-ethylmaleimide, which indicates that a gamma-type DNA polymerase was responsible for this activity. Mitochondrial nucleoids were capable of self-directed RNA transcription in a non-random fashion in vitro. Consistent with and complementary to results from fungi and human cells done mostly in situ, our present work helps to establish the important paradigm that mitochondrial nucleoids in eukaryotes are more than mere mtDNA compaction and segregation entities but are centers of mtDNA maintenance and expression.
机译:从绿豆幼苗分离的线粒体类核苷显示出与膜成分相关的染色质样结构。在子叶发育期间经历了离散变化的相似结构被原位鉴定。分离的核苷由基本相同的磷脂(包括心磷脂)组成,包括完整的线粒体以及线粒体内膜和内膜的蛋白质。肌动蛋白一直被发现与用不同去污剂浓度制备的线粒体核苷酸相似。甲醛与细胞松弛素B和蛋白酶K处理的线粒体的交联进一步揭示肌动蛋白与核苷中的DNA有关。线粒体的类核苷酸在模拟分离的线粒体中mtDNA合成的模式中可以自给自足地指导体外DNA合成。在脉冲场凝胶电泳中,新合成的mtDNA分为两个主要部分,即结合良好和快速移动的形式。核仁DNA合成对蚜虫碱有抗性,但对N-乙基马来酰亚胺敏感,这表明γ型DNA聚合酶是这种活性的原因。线粒体类核苷酸能够以非随机方式在体外自我指导RNA转录。与大多数原位完成的真菌和人类细胞的结果一致并相互补充,我们目前的工作有助于建立一个重要的范式,即真核生物中的线粒体核苷酸不仅是mtDNA的紧缩和分离实体,而且是mtDNA维持和表达的中心。

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