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相关概念视频

Bacterial RNA Polymerase00:43

Bacterial RNA Polymerase

Unlike eukaryotes, bacteria use a single RNA Polymerase (RNAP) to transcribe all genes. The different subunits of bacterial RNAPhave distinct functions. The multisubunit structure of the bacterial RNAP helps the enzyme to maintain catalytic function, facilitate assembly, interact with DNA and RNA, and self-regulate its activity.
In most genes, the transcription site is a single base present upstream of the coding sequence. Though RNAP is a catalytically efficient enzyme, it does not recognize...
RNA Polymerase II Accessory Proteins02:36

RNA Polymerase II Accessory Proteins

Proteins that regulate transcription can do so either via direct contact with RNA Polymerase or through indirect interactions facilitated by adaptors, mediators, histone-modifying proteins, and nucleosome remodelers. Direct interactions to activate transcription is seen in bacteria as well as in some eukaryotic genes. In these cases, upstream activation sequences are adjacent to the promoters, and the activator proteins interact directly with the transcriptional machinery. For example, in...
Ribosomal RNA Synthesis02:53

Ribosomal RNA Synthesis

Ribosome synthesis is a highly complex and coordinated process involving more than 200 assembly factors. The synthesis and processing of ribosomal components occurs not only in the nucleolus but also in the nucleoplasm and the cytoplasm of eukaryotic cells.
Ribosome biogenesis begins with the synthesis of 5S and 45S pre-rRNAs by distinct RNA polymerases. The primary transcripts are extensively processed and modified before they are bound and folded by ribosomal proteins and assembly factors,...
Cooperative Binding of Transcription Regulators02:13

Cooperative Binding of Transcription Regulators

Transcriptional regulators bind to specific cis-regulatory sequences in the DNA to regulate gene transcription. These cis-regulatory sequences are very short, usually less than ten nucleotide pairs in length. The short length means that there is a high probability of the exact same sequence randomly occurring throughout the genome.  Since regulators can also bind to groups of similar sequences, this further increases the chances of random binding. Transcriptional regulators form dimers that...
piRNA - Piwi-interacting RNAs02:57

piRNA - Piwi-interacting RNAs

PIWI-interacting RNAs, or piRNAs, are the most abundant short non-coding RNAs. More than 20,000 genes have been found in humans that code for piRNAs while only 2000 genes have been found for miRNAs. piRNAs can act at the transcriptional and post-transcriptional levels and have a vital role in silencing transposable elements present in germ cells. They are also involved in epigenetic silencing and activation. Previously, they were thought to function only in germ cells but new evidence suggests...
RNA Polymerase II Accessory Proteins02:36

RNA Polymerase II Accessory Proteins

Proteins that regulate transcription can do so either via direct contact with RNA Polymerase or through indirect interactions facilitated by adaptors, mediators, histone-modifying proteins, and nucleosome remodelers. Direct interactions to activate transcription is seen in bacteria as well as in some eukaryotic genes. In these cases, upstream activation sequences are adjacent to the promoters, and the activator proteins interact directly with the transcriptional machinery. For example, in...

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相关实验视频

Updated: Jul 8, 2026

Isolation of Cognate RNA-protein Complexes from Cells Using Oligonucleotide-directed Elution
10:53

Isolation of Cognate RNA-protein Complexes from Cells Using Oligonucleotide-directed Elution

Published on: January 16, 2017

两个RNAi复合体,RITS和RDRC,在物理上相互作用并局部化为非编码的中心基RNAs.

Mohammad R Motamedi1, André Verdel, Serafin U Colmenares

  • 1Department of Cell Biology, Harvard Medical School, Boston, MA 02115, USA.

Cell
|December 21, 2004
PubMed
概括

以RNA为导向的RNA聚合酶复合体 (RDRC) 在物理和功能上与RNA诱导的转录沉默 (RITS) 复合体结合. 这种相互作用对于裂变酵母中siRNA依赖的异染色素组合至关重要.

科学领域:

  • 表观遗传学 在表观遗传学中,表观遗传学是指表观遗传学.
  • RNA干扰 (RNAi) 是一种RNA干扰.
  • 分子生物学分子生物学

背景情况:

  • 通过RNAi介导的异染色蛋白组合需要RITS复合体和Rdp1.1.
  • 在这个过程中,Rdp1的确切功能和相互作用尚未完全理解.

研究的目的:

  • 阐明Rdp1在异色染色体组合中的分子相互作用和功能意义.
  • 描述由Rdp1及其相关蛋白质形成的复合体.

主要方法:

  • 共同免疫沉以识别相互作用的蛋白质复合体.
  • 使用显微镜分析蛋白质定位.
  • 在淘汰菌株中进行siRNA分析.
  • 对RNA指导的RNA聚合酶活性进行检测.

主要成果:

  • Rdp1与Hrr1 (RNA基酶) 和Cid12 (polyA聚合酶) 形成一个复合体 (RDRC),具有RNA指导的RNA聚合酶活性.
  • RDRC与RITS相互作用,需要Dicer (Dcr1) 和Clr4.
  • 无论是RDRC还是RITS都定位在核中,并以Dcr1-依赖的方式与中心RNA结合.
  • 丢失Rdp1,Hrr1或Cid12导致RITS缺少siRNA并无法定位到中心重复.

更多相关视频

Novel RNA-Binding Proteins Isolation by the RaPID Methodology
11:19

Novel RNA-Binding Proteins Isolation by the RaPID Methodology

Published on: September 30, 2016

RNA-Associated Chromatin DNA-DNA Interaction Method
11:01

RNA-Associated Chromatin DNA-DNA Interaction Method

Published on: April 30, 2026

相关实验视频

Last Updated: Jul 8, 2026

Isolation of Cognate RNA-protein Complexes from Cells Using Oligonucleotide-directed Elution
10:53

Isolation of Cognate RNA-protein Complexes from Cells Using Oligonucleotide-directed Elution

Published on: January 16, 2017

Novel RNA-Binding Proteins Isolation by the RaPID Methodology
11:19

Novel RNA-Binding Proteins Isolation by the RaPID Methodology

Published on: September 30, 2016

RNA-Associated Chromatin DNA-DNA Interaction Method
11:01

RNA-Associated Chromatin DNA-DNA Interaction Method

Published on: April 30, 2026

结论:

  • 在Rdp1和RITS复合体之间存在物理和功能联系.
  • 非编码RNA作为一个平台,用于siRNA依赖的RNAi机械的定位到特定的基因组区域.
  • 这项研究揭示了一种由RNA指导的RNA聚合酶活性和RITS介导的异染色蛋白形成的新机制.