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相关概念视频

RNA Splicing01:32

RNA Splicing

Splicing is the process by which eukaryotic RNA is edited before its translation into protein. The RNA strand transcribed from eukaryotic DNA is called the primary transcript. The primary transcripts that become mRNAs are called precursor messenger RNAs (pre-mRNAs). Eukaryotic pre-mRNA contains alternating sequences of exons and introns. Exons are nucleotide sequences that code for proteins, whereas introns are the non-coding regions. In RNA splicing, introns are removed and exons are bonded...
Translesion DNA Polymerases02:10

Translesion DNA Polymerases

Translesion (TLS) polymerases rescue stalled DNA polymerases at sites of damaged bases by replacing the replicative polymerase and installing a nucleotide across the damaged site. Doing so, TLS allows additional time for the cell to repair the damage before resuming regular DNA replication.
TLS polymerases are found in all three domains of life - archaea, bacteria, and eukaryotes. Of the different classes of TLS polymerases, members of the Y family are fitted with specialized structures that...
RNA Splicing01:32

RNA Splicing

Splicing is the process by which eukaryotic RNA is edited before its translation into protein. The RNA strand transcribed from eukaryotic DNA is called the primary transcript. The primary transcripts that become mRNAs are called precursor messenger RNAs (pre-mRNAs). Eukaryotic pre-mRNA contains alternating sequences of exons and introns. Exons are nucleotide sequences that code for proteins, whereas introns are the non-coding regions. In RNA splicing, introns are removed and exons are bonded...
PCR - Polymerase Chain Reaction01:32

PCR - Polymerase Chain Reaction

Overview
Restriction Enzymes01:11

Restriction Enzymes

Restriction enzymes are bacterial enzymes used to cut DNA in a sequence-specific manner. To cleave DNA, they bind to specific palindromic sequences called restriction sites. Such palindromic DNA sequences or inverted repeats are commonly found in regions of functional significance, such as the origin of replication, gene operator sites, and regions containing transcription termination signals.
The host bacteria protect their own genomic DNA from these enzymes by methylating these sites. Some...
DNA Bacteriophages01:26

DNA Bacteriophages

Bacteriophages, or phages, are viruses that specifically infect bacteria, utilizing their genetic material to hijack host cellular machinery for replication. DNA bacteriophages employ single-stranded DNA (ssDNA) or double-stranded DNA (dsDNA) genomes. These phages exhibit diverse replication strategies and host interactions, influencing their ecological roles and applications in biotechnology and medicine.ssDNA BacteriophagesssDNA phages, with their small genomes, utilize unique strategies to...

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相关实验视频

Updated: Jun 24, 2026

Generation of RNA/DNA Hybrids in Genomic DNA by Transformation using RNA-containing Oligonucleotides
16:42

Generation of RNA/DNA Hybrids in Genomic DNA by Transformation using RNA-containing Oligonucleotides

Published on: November 25, 2010

通过具有扩展化学功能的DNA酶进行RNA裂变.

S W Santoro1, G F Joyce, K Sakthivel

  • 1Department of Chemistry, The Scripps Research Institute, La Jolla, California 92037, USA.

Journal of the American Chemical Society
|September 7, 2001
PubMed
概括

研究人员使用体外选择开发了一种小型DNA酶. 这种多功能酶有效地使用必不可少的伊米达群和Zn2+催化剂切割RNA基质.

科学领域:

  • 生物化学 生物化学
  • 分子生物学分子生物学
  • 合成生物学 合成生物学

背景情况:

  • 基因酶或脱氧酶为新型催化应用提供了潜在的潜力.
  • 将功能组集成到核酸中是扩大其催化能力的关键.

研究的目的:

  • 开发一种具有伊米达功能的新型DNA酶,用于RNA裂变.
  • 为了设计一个小的,多功能,并具有催化效率的核酸酶.

主要方法:

  • 在体外选择使用含有意达功能化脱氧氨的改性核酸库.
  • 化学合成来定义一个最小的12个残留的催化域.
  • 酶动力学和基质特异性的表征.

主要成果:

  • 成功开发了一种具有三种催化必需的伊米达群的DNA酶.
  • 最小化的催化域形成了一个针头结构,显示RNA裂变的伊米达残留物.
  • 该酶证明了高效的多重循环催化 (>1分钟-1) 与Zn2+和和动力学.
  • 基质特异性可以通过修改基质识别域来轻松改变.

结论:

  • 创建了一个小型多功能DNA酶,将核酸识别与类似蛋白质的化学功能相结合.

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Using Modified Synthetic Oligonucleotides to Assay Nucleic Acid-Metabolizing Enzymes

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相关实验视频

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Generation of RNA/DNA Hybrids in Genomic DNA by Transformation using RNA-containing Oligonucleotides
16:42

Generation of RNA/DNA Hybrids in Genomic DNA by Transformation using RNA-containing Oligonucleotides

Published on: November 25, 2010

DNAzyme-dependent Analysis of rRNA 2&#8217;-O-Methylation
09:12

DNAzyme-dependent Analysis of rRNA 2’-O-Methylation

Published on: September 16, 2019

Using Modified Synthetic Oligonucleotides to Assay Nucleic Acid-Metabolizing Enzymes
05:33

Using Modified Synthetic Oligonucleotides to Assay Nucleic Acid-Metabolizing Enzymes

Published on: July 5, 2024

  • 这种含有伊米达的DNA酶代表了核酸酶工程的重大进展.
  • 开发的DNA酶非常高效,可以适应分裂各种RNA序列.