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関連する概念動画

Gene Evolution - Fast or Slow?02:05

Gene Evolution - Fast or Slow?

The genomes of eukaryotes are punctuated by long stretches of sequence which do not code for proteins or RNAs. Although some of these regions do contain crucial regulatory sequences, the vast majority of this DNA serves no known function. Typically, these regions of the genome are the ones in which the fastest change, in evolutionary terms, is observed, because there is typically little to no selection pressure acting on these regions to preserve their sequences.
In contrast, regions which code...
Non-LTR Retrotransposons03:18

Non-LTR Retrotransposons

As the name suggests, non-LTR retrotransposons lack the long terminal repeats characteristic of the LTR retrotransposons. Additionally, both LTR and non-LTR retrotransposons use distinct mechanisms of mobilization. Non-LTR retrotransposons are further divided into two classes - Long interspersed nuclear elements (LINEs) and short interspersed nuclear elements (SINEs), both of which occur abundantly in most mammals, including humans. Some of the active non-LTR retrotransposons in humans are L1...
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...
Bacterial Transcription01:53

Bacterial Transcription

RNA polymerase (RNAP) carries out DNA-dependent RNA synthesis in both bacteria and eukaryotes. Bacteria do not have a membrane-bound nucleus. So, transcription and translation occur simultaneously, on the same DNA template.
Transcription can be divided into three main stages, each involving distinct DNA sequences to guide the polymerase. These are:
Gene Evolution - Fast or Slow?02:05

Gene Evolution - Fast or Slow?

The genomes of eukaryotes are punctuated by long stretches of sequence which do not code for proteins or RNAs. Although some of these regions do contain crucial regulatory sequences, the vast majority of this DNA serves no known function. Typically, these regions of the genome are the ones in which the fastest change, in evolutionary terms, is observed, because there is typically little to no selection pressure acting on these regions to preserve their sequences.
In contrast, regions which code...
Pre-mRNA Processing: Modification of pre-mRNA Ends01:35

Pre-mRNA Processing: Modification of pre-mRNA Ends

In eukaryotic cells, transcripts made by RNA polymerase are modified and processed before exiting the nucleus. Unprocessed RNA is called precursor mRNA or pre-mRNA to distinguish it from mature mRNA.
Once about 20-40 ribonucleotides have been joined together by RNA polymerase, a group of enzymes adds a cap to the 5' end of the growing transcript. In this process, a 5' phosphate is replaced by modified guanosine that has a methyl group attached (7-methyl guanosine). This 5' cap helps the cell...

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関連する実験動画

Updated: Jun 28, 2026

Assessment of DNA Contamination in RNA Samples Based on Ribosomal DNA
13:16

Assessment of DNA Contamination in RNA Samples Based on Ribosomal DNA

Published on: January 22, 2018

人間のRap1の識別:テロメアの進化への影響

B Li1, S Oestreich, T de Lange

  • 1The Rockefeller University, New York, New York 10021, USA.

Cell
|June 13, 2000
PubMed
まとめ

研究者らは,ヒトのRap1 (hRap1) を酵母Rap1.1にオーソログなテロメアタンパク質として特定した. この発見は,芽生えた酵母にいくつかの哺乳類のテロメアタンパク質が存在しないことを説明し,テロメア成分が進化的に保存されていることを示唆しています.

科学分野:

  • 分子生物学は分子生物学である.
  • 遺伝学 遺伝学とは
  • 細胞生物学 細胞生物学

背景:

  • 哺乳類のテロメアには,TRF1,TRF2,タンキラーゼ,TIN2などのタンパク質が含まれており,芽生える酵母には明確な対称がない.
  • 異なる酵母種と哺乳類におけるテロメアタンパク質の進化的関係は,まだ完全に理解されていません.

研究 の 目的:

  • 哺乳類および分裂酵母における酵母テロメアタンパク質のオーソログを特定し,特徴づけること.
  • テロメアタンパク質複合体の進化史と保存の解明.

主な方法:

  • 人間と酵母間の保存モチーフを特定するためのシーケンスホモロジー分析 Rap1.1.
  • セルラー画像技術を用いたテロメア局所化研究.
  • テロメア長さの維持に与える影響を評価するための機能検査.

主要な成果:

  • ヒトのタンパク質であるhRap1は,発芽中の酵母テロメアタンパク質scRap1pのオートログとして識別され,保存された配列モチーフを共有しています.
  • hRap1はテロメアに局所化し,テロメアの長さに影響を与えますが,scRap1pとは異なり,TRF2によって採用されます.
  • 分裂酵母タンパク質Taz1は,TRFのオルトログとして識別され,TRFの保存を示した.

さらに関連する動画

Using the E1A Minigene Tool to Study mRNA Splicing Changes
10:25

Using the E1A Minigene Tool to Study mRNA Splicing Changes

Published on: April 22, 2021

Development and Application of Rapamycin-regulated Tyrosine Phosphatases
06:56

Development and Application of Rapamycin-regulated Tyrosine Phosphatases

Published on: September 6, 2024

関連する実験動画

Last Updated: Jun 28, 2026

Assessment of DNA Contamination in RNA Samples Based on Ribosomal DNA
13:16

Assessment of DNA Contamination in RNA Samples Based on Ribosomal DNA

Published on: January 22, 2018

Using the E1A Minigene Tool to Study mRNA Splicing Changes
10:25

Using the E1A Minigene Tool to Study mRNA Splicing Changes

Published on: April 22, 2021

Development and Application of Rapamycin-regulated Tyrosine Phosphatases
06:56

Development and Application of Rapamycin-regulated Tyrosine Phosphatases

Published on: September 6, 2024

結論:

  • この発見は,祖先のテロメアにはTRFのようなタンパク質と脊椎動物に似たRap1の両方が含まれていたことを示唆している.
  • 芽生える酵母は,TRF成分を失う一方でテロメアでRap1を保持している可能性があり,テロメアの繰り返し配列の変化に潜在的に関連しています.