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相关概念视频

Riboswitches01:56

Riboswitches

Riboswitches are non-coding mRNA domains that regulate the transcription and translation of downstream genes without the help of proteins. Riboswitches bind directly to a metabolite and can form unique stem-loop or hairpin structures in response to the amount of the metabolite present. They have two distinct regions – a metabolite-binding aptamer and an expression platform.
The aptamer has high specificity for a particular metabolite which allows riboswitches to specifically regulate...
Leaky Scanning02:28

Leaky Scanning

During most eukaryotic translation processes, the small 40S ribosome subunit scans an mRNA from its 5' end until it encounters the first start AUG codon. The large 60S ribosomal subunit then joins the smaller one to initiate protein synthesis. The location of the translation initiation is largely determined by the nucleotides near the start codon as there may be multiple translation initiation sites present on the mRNA.  Marilyn Kozak discovered that the sequence RCCAUGG (where R stands for...
Rab Proteins01:14

Rab Proteins

Rab proteins constitute the largest family of monomeric GTPases, of which 70 members are present in humans. Rab proteins and their effectors regulate consecutive stages of vesicle transport such as vesicle transport, docking, and fusion to the correct recipient membrane.
Rab proteins switch between a cytosolic, GDP-bound inactive state and a membrane-anchored, GTP-bound active state. By themselves, Rabs show slow rates of GDP/GTP exchange and GTP hydrolysis. Thus, Rab proteins are considered...
Regulation of Expression at Multiple Steps01:23

Regulation of Expression at Multiple Steps

The gene expression in cells is regulated at different stages: (i) transcription, (ii) RNA processing, (iii) RNA localization, and (iv) translation. Transcriptional regulation is mediated by regulatory proteins such as transcription factors, activators, or repressors—these control gene expression by initiating or inhibiting the transcription of genes. Once a precursor or pre-mRNA is produced, it undergoes post-transcriptional modification, including 5' capping, splicing, and the addition of a...

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相关实验视频

Updated: Jul 12, 2026

Genome-wide Analysis using ChIP to Identify Isoform-specific Gene Targets
11:19

Genome-wide Analysis using ChIP to Identify Isoform-specific Gene Targets

Published on: July 7, 2010

通过RAG2的细胞类型特定DNA元素5'对RAG1和RAG2进行协调调节.

W Yu1, Z Misulovin, H Suh

  • 1Laboratory of Molecular Immunology, Rockefeller University, 1230 York Avenue, New York, NY 10021, USA.

Science (New York, N.Y.)
|August 14, 1999
PubMed
概括

这项研究研究了RAG1和RAG2基因的调节,这对淋巴细胞发育至关重要. 控制它们表达的独特遗传元素表明它们融入脊椎动物进化的机制.

科学领域:

  • 免疫学 免疫学 免疫学
  • 分子生物学分子生物学
  • 进化生物学 进化生物学

背景情况:

  • RAG1和RAG2蛋白对于V(D) J重组是必不可少的,这是适应性免疫的关键过程.
  • 假设这些基因起源于数百万年前融入脊椎动物基因组的移动遗传元件.

研究的目的:

  • 为了研究RAG1和RAG2基因表达的体内调节.
  • 确定控制RAG1和RAG2在发育中的淋巴细胞中的坐标表达的遗传元素.

主要方法:

  • 利用带有光指示器的细菌人造染色体 (BAC) 转基因来跟踪体内基因表达.
  • 分析了RAG2基因上游的调节区域,以确定cis作用元素.

主要成果:

  • 在B和T淋巴细胞中展示了RAG1和RAG2的坐标表达.
  • 确定了位于RAG2基因5'侧的独特遗传元素,这些元素调节了这个坐标表达.

结论:

  • 表明不对称地放置的cis DNA元素控制了祖先转子子的表达.
  • 提出了一种机制,这些调节元素促进了脊椎动物RAG基因的捕获和进化.

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Prediction and Validation of Gene Regulatory Elements Activated During Retinoic Acid Induced Embryonic Stem Cell Differentiation
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Prediction and Validation of Gene Regulatory Elements Activated During Retinoic Acid Induced Embryonic Stem Cell Differentiation

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

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相关实验视频

Last Updated: Jul 12, 2026

Genome-wide Analysis using ChIP to Identify Isoform-specific Gene Targets
11:19

Genome-wide Analysis using ChIP to Identify Isoform-specific Gene Targets

Published on: July 7, 2010

Prediction and Validation of Gene Regulatory Elements Activated During Retinoic Acid Induced Embryonic Stem Cell Differentiation
09:07

Prediction and Validation of Gene Regulatory Elements Activated During Retinoic Acid Induced Embryonic Stem Cell Differentiation

Published on: June 21, 2016

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