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相关概念视频

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,...
Ribosome Profiling02:24

Ribosome Profiling

Ribosome profiling or ribo-sequencing is a deep sequencing technique that produces a snapshot of active translation in a cell. It selectively sequences the mRNAs protected by ribosomes to get an insight into a cell’s translation landscape at any given point in time.
Applications of ribosome profiling
Ribosome profiling has many applications, including in vivo monitoring of translation inside a particular organ or tissue type and quantifying new protein synthesis levels.
The technique helps...
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,...
Prokaryotic Gene Structure and Organization01:28

Prokaryotic Gene Structure and Organization

Prokaryotic genomes exhibit a streamlined organization of coding and non-coding regions essential for gene expression and protein synthesis. While coding regions contain the genetic instructions for proteins or functional RNAs, non-coding regions regulate the precise transcription and translation of these genes.Coding Regions: Proteins and RNAsThe primary coding regions, known as structural genes, include sequences transcribed into messenger RNA (mRNA) and ultimately translated into...
Transcription in Prokaryotes01:28

Transcription in Prokaryotes

Transcription is a highly regulated process that converts genetic information into RNA molecules. The transcription cycle is divided into three key stages: initiation, elongation, and termination, each driven by specific molecular mechanisms.Initiation of TranscriptionIn bacteria, transcription begins when the RNA polymerase core enzyme associates with a sigma factor to form a holoenzyme. For example, the E. coli sigma factor called σ70 forms a holoenzyme, which recognizes the -10 (Pribnow box)...
Three-Domain System of Life01:21

Three-Domain System of Life

Ribosomal RNA (rRNA) sequence analysis revealed three distinct groups of cells: eukaryotes, bacteria, and archaea. In 1978, Carl R. Woese proposed the concept of domains, a taxonomic level above kingdoms, to differentiate these groups. He suggested that archaea and bacteria, despite their similar appearance, represent separate domains. Domains differ in rRNA, membrane lipid structure, transfer RNA, and antibiotic sensitivity.In this classification, animals, plants, and fungi belong to the...

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相关实验视频

Updated: Jul 6, 2026

High-throughput Measurement of Dictyostelium discoideum Macropinocytosis by Flow Cytometry
06:47

High-throughput Measurement of Dictyostelium discoideum Macropinocytosis by Flow Cytometry

Published on: September 10, 2018

迪西奥斯泰利姆迪斯科伊德 (Dictyostelium discoideum) 的核糖体RNA基因的组织:绘制非转录的间隔区域的映射.

A F Cockburn, M J Newkirk, R A Firtel

    Cell
    |December 1, 1976
    PubMed
    概括

    双胞胎核糖体DNA (rDNA) 重复单元至少长42kb,其中8kb编码rRNA前体. 映射显示了同质的限制片段,表明非转录间隔器内的复杂结构安排.

    科学领域:

    • 分子生物学分子生物学
    • 遗传学 是一个遗传学.
    • 细胞生物学 细胞生物学

    背景情况:

    • 核糖体DNA (rDNA) 的组织对于细胞功能至关重要.
    • 了解Dictyostelium discoideum中非转录间隔器 (NTS) 的结构是理解rDNA调节的关键.
    • 之前的研究已经开始对DictyosteliumrDNA进行映射.

    研究的目的:

    • 为了映射Dictyostelium中的核糖体非转录间隔DNA.
    • 描述重复单元及其在rDNA位置内的组织.
    • 确定由rDNA构成的核DNA的比例.

    主要方法:

    • 使用Eco R1,Hind III和Sal I酶进行限制消化.
    • 对含有rDNA部分的重组等离子体的分析.
    • 重复单位和编码区域的尺寸确定.

    主要成果:

    • 核糖体DNA重复单位至少长42千基 (kb).
    • 每个重复单元中的大约8kb编码了36SrRNA前体.
    • 限制消化结果呈现出同质的模式,表明重复单元内保存的序列.

    更多相关视频

    Genetic Engineering of Dictyostelium discoideum Cells Based on Selection and Growth on Bacteria
    06:08

    Genetic Engineering of Dictyostelium discoideum Cells Based on Selection and Growth on Bacteria

    Published on: January 25, 2019

    Single Nucleotide Polymorphism-sensitive FISH Detection of Locus-specific Ribosomal RNA Transcription in Drosophila melanogaster
    04:59

    Single Nucleotide Polymorphism-sensitive FISH Detection of Locus-specific Ribosomal RNA Transcription in Drosophila melanogaster

    Published on: March 28, 2025

    相关实验视频

    Last Updated: Jul 6, 2026

    High-throughput Measurement of Dictyostelium discoideum Macropinocytosis by Flow Cytometry
    06:47

    High-throughput Measurement of Dictyostelium discoideum Macropinocytosis by Flow Cytometry

    Published on: September 10, 2018

    Genetic Engineering of Dictyostelium discoideum Cells Based on Selection and Growth on Bacteria
    06:08

    Genetic Engineering of Dictyostelium discoideum Cells Based on Selection and Growth on Bacteria

    Published on: January 25, 2019

    Single Nucleotide Polymorphism-sensitive FISH Detection of Locus-specific Ribosomal RNA Transcription in Drosophila melanogaster
    04:59

    Single Nucleotide Polymorphism-sensitive FISH Detection of Locus-specific Ribosomal RNA Transcription in Drosophila melanogaster

    Published on: March 28, 2025

  • 总的rDNA至少占Dictyostelium核DNA的18%.
  • 结论:

    • 在Dictyostelium的rDNA重复单元表现出一个保存的结构.
    • 非转录的间隔器可能包含异质区域或复杂的链接安排.
    • rDNA代表了Dictyostelium基因组的很大一部分.