Jove
Visualize
联系我们
JoVE
x logofacebook logolinkedin logoyoutube logo
关于 JoVE
概览领导团队博客JoVE 帮助中心
作者
出版流程编辑委员会范围与政策同行评审常见问题投稿
图书馆员
用户评价订阅访问资源图书馆顾问委员会常见问题
研究
JoVE JournalMethods CollectionsJoVE Encyclopedia of Experiments存档
教育
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab Manual教师资源中心教师网站
使用条款与条件
隐私政策
政策

相关概念视频

Cis-regulatory Sequences02:02

Cis-regulatory Sequences

9.8K
Cis-regulatory sequences are short fragments of non-coding DNA that are present on the same chromosomes as the genes that they regulate. These fragments serve as binding sites for transcriptional regulators, proteins that are responsible for controlling gene transcription and differential gene expression across cell types in eukaryotes. Cis-regulatory sequences can be close to the gene of interest or thousands of bases away in the DNA sequence; however, those sequences that are further away are...
9.8K
Regulation of Expression at Multiple Steps01:23

Regulation of Expression at Multiple Steps

886
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...
886
Cooperative Binding of Transcription Regulators02:13

Cooperative Binding of Transcription Regulators

6.4K
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...
6.4K
Regulation of Expression Occurs at Multiple Steps02:24

Regulation of Expression Occurs at Multiple Steps

22.6K
Gene expression can be regulated at almost every step from gene to protein. Transcription is the step that is most commonly regulated. This involves the binding of proteins to short regulatory sequences on the DNA. This association can either promote or inhibit the transcription of a gene associated with the respective sequence.
Transcription results in the generation of precursor (pre-mRNA) that consists of both exons and introns, which needs further processing before being translated to a...
22.6K
General Transcription Factors01:30

General Transcription Factors

5.2K
Tissue-specific transcription factors contribute to diverse cellular functions in mammals. For example, the gene for beta globin, a major component of hemoglobin, is present in all cells of the body. However, it is only expressed in red blood cells because the transcription factors that can bind to the promoter sequences of the beta globin gene are only expressed in these cells. Tissue-specific transcription factors also ensure that mutations in these factors may impair only the function of...
5.2K
Co-activators and Co-repressors02:04

Co-activators and Co-repressors

7.3K
Gene transcription is regulated by the synergistic action of several proteins that form a complex at a gene regulatory site. This is observed in eukaryotes, where the regulation of gene expression is a complex process. Regulatory proteins in eukaryotes can broadly be classified into two types – regulators that bind directly to specific DNA sequences and co-regulators that associate with regulatory proteins but cannot directly bind to the DNA. These co-regulators are further divided into...
7.3K

您也可能阅读

相关文章

通过共同作者、期刊和引用图与本文相关的文章。

排序
Same author

Therapeutic potential of dihydronicotinamide riboside (NRH) on obesity and glucose intolerance in mice.

Nature communications·2026
Same author

Decoding the immune-tumor synapse for data-driven design of next-generation immunotherapies.

Trends in immunology·2026
Same author

MEDAG functions as an A-kinase-anchoring protein in adipocytes.

Molecular cell·2026
Same author

Cell surface interactome analysis identifies TSPAN4 as a negative regulator of PD-L1 in melanoma.

Molecular oncology·2026
Same author

Designing synthetic regulatory elements using the generative AI framework DNA-Diffusion.

Nature genetics·2025
Same author

Innate type 2 lymphocytes trigger an inflammatory switch in alveolar macrophages.

Immunity·2025

相关实验视频

Updated: Jun 20, 2025

Author Spotlight: An Integrated Workflow to Study the Promoter-Centric Spatio-Temporal Genome Architecture in Scarce Cell Populations
11:36

Author Spotlight: An Integrated Workflow to Study the Promoter-Centric Spatio-Temporal Genome Architecture in Scarce Cell Populations

Published on: April 21, 2023

2.0K

非编码变体以特定细胞类型的方式影响 cis 调控协调.

Olga Pushkarev1,2, Guido van Mierlo3,4, Judith Franziska Kribelbauer1,2

  • 1Laboratory of Systems Biology and Genetics, Institute of Bioengineering, School of Life Sciences, École Polytechnique Fédérale de Lausanne (EPFL), Lausanne, Switzerland.

Genome biology
|July 18, 2024
PubMed
概括

这项研究优化了绘制染色体模块 (CMs) 的方法,染色体模块是相互作用的cis调节元件 (CREs) 的组. 这些CM揭示了基因变异如何以细胞类型特定的方式影响基因表达和疾病风险.

关键词:
关键调节性相互作用表观基因组学是指表观基因组学.基因调节 基因调节全基因组关联研究研究.定量性特征位置 (loci loci) 是一个定量性特征位置.

更多相关视频

Screening for Functional Non-coding Genetic Variants Using Electrophoretic Mobility Shift Assay EMSA and DNA-affinity Precipitation Assay DAPA
11:35

Screening for Functional Non-coding Genetic Variants Using Electrophoretic Mobility Shift Assay EMSA and DNA-affinity Precipitation Assay DAPA

Published on: August 21, 2016

12.9K
HOX Loci Focused CRISPR/sgRNA Library Screening Identifying Critical CTCF Boundaries
10:10

HOX Loci Focused CRISPR/sgRNA Library Screening Identifying Critical CTCF Boundaries

Published on: March 31, 2019

8.3K

相关实验视频

Last Updated: Jun 20, 2025

Author Spotlight: An Integrated Workflow to Study the Promoter-Centric Spatio-Temporal Genome Architecture in Scarce Cell Populations
11:36

Author Spotlight: An Integrated Workflow to Study the Promoter-Centric Spatio-Temporal Genome Architecture in Scarce Cell Populations

Published on: April 21, 2023

2.0K
Screening for Functional Non-coding Genetic Variants Using Electrophoretic Mobility Shift Assay EMSA and DNA-affinity Precipitation Assay DAPA
11:35

Screening for Functional Non-coding Genetic Variants Using Electrophoretic Mobility Shift Assay EMSA and DNA-affinity Precipitation Assay DAPA

Published on: August 21, 2016

12.9K
HOX Loci Focused CRISPR/sgRNA Library Screening Identifying Critical CTCF Boundaries
10:10

HOX Loci Focused CRISPR/sgRNA Library Screening Identifying Critical CTCF Boundaries

Published on: March 31, 2019

8.3K

科学领域:

  • 基因组学就是基因组学.
  • 表观遗传学 在表观遗传学中,表观遗传学是指表观遗传学.
  • 基因规则 基因规则

背景情况:

  • 对基因调节至关重要的是Cis调节元素 (CRE) 相互作用.
  • 染色体模块 (CMs) 使用表观基因组变异映射这些相互作用.
  • 现有的CM映射计算方法的结果各不相同.

研究的目的:

  • 评估和完善CM映射工具,以实现最佳的表观基因组数据利用.
  • 评估人类基因组中的监管协调.
  • 了解CMs对基因表达和疾病倾向的影响.

主要方法:

  • 综合评估和简化现有的CM映射工具.
  • 分析来自不同种群和不同细胞类型的表观基因组数据.
  • 整合基因型信息以确定非编码变异的影响.

主要成果:

  • 开发了使用多种表观基因组数据进行最佳CM绘制的指导方针.
  • 在CM中展示了细胞类型特定的CRE相互作用及其与基因表达的联系.
  • 展示了非编码变异如何以特定细胞类型的方式影响CM活性和转录因子结合.
  • 在解构GWAS位点,分析免疫细胞受体和理解白血病预后标志物方面,插图CM应用.

结论:

  • 建立了CM映射的最佳策略,捕捉了CRE协调及其对基因表达的影响.
  • 非编码的遗传变异可以破坏CRE协调,可能导致细胞类型特定的疾病倾向.