Jove
Visualize
お問い合わせ
JoVE
x logofacebook logolinkedin logoyoutube logo
JoVEについて
概要リーダーシップブログJoVEヘルプセンター
著者向け
出版プロセス編集委員会範囲と方針査読よくある質問投稿
図書館員向け
推薦の声購読アクセスリソース図書館諮問委員会よくある質問
研究
JoVE JournalMethods CollectionsJoVE Encyclopedia of Experimentsアーカイブ
教育
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab Manual教員リソースセンター教員サイト
利用規約
プライバシーポリシー
ポリシー

関連する概念動画

Viral Mutations00:36

Viral Mutations

A mutation is a change in the sequence of bases of DNA or RNA in a genome. Some mutations occur during replication of the genome due to errors made by the polymerase enzymes that replicate DNA or RNA. Unlike DNA polymerase, RNA polymerase is prone to errors because it is not capable of “proofreading” its work. Viruses with RNA-based genomes, like HIV, therefore accrue mutations faster than viruses with DNA-based genomes. Because mutation and recombination provide the raw material for adaptive...
Conservative Site-specific Recombination and Phase Variation02:53

Conservative Site-specific Recombination and Phase Variation

Because the DNA segments are cut and reorganized in a direction-specific manner, site-specific recombination has emerged as an efficient genetic engineering technique. Flippase and Cyclization recombinases or Flp and Cre, respectively, are two members of the tyrosine recombinase family derived from bacteriophages, that are used to mediate site-specific DNA insertions, deletions, and targeted expression of proteins in mammalian cell lines.
The recognition sites for Cre recombinase called LoxP...
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...
Point and Frameshift Mutations01:30

Point and Frameshift Mutations

Point mutations are genetic alterations involving the change of a single nucleotide base pair in DNA. Depending on how the alteration affects protein synthesis, they can lead to various consequences.Point mutations fall into the following types:Silent mutations occur when a nucleotide change does not alter the amino acid sequence due to the redundancy of the genetic code. For instance, changing ACC to ACA still encodes threonine, leaving the protein function unaffected. This occurs because...
Size and Structure of Viral Genomes01:26

Size and Structure of Viral Genomes

Viral genomes exhibit remarkable diversity in size, structure, and composition, influencing their replication strategies and interactions with host cells. These genomes consist of either DNA or RNA and may be linear or circular. Additionally, they can be single-stranded or double-stranded, with each configuration affecting how the virus propagates within a host. RNA viruses, for instance, generally have smaller genomes than DNA viruses, a factor that contributes to their high mutation rates and...
Viruses with RNA Genomes01:29

Viruses with RNA Genomes

RNA viruses are categorized into positive-strand, negative-strand, or double-stranded groups based on their genomic structure and replication mechanisms. This classification dictates how they exploit host cellular machinery for protein synthesis and replication. Some RNA viruses also utilize reverse transcription as part of their life cycle, further diversifying their replication strategies.Positive-Strand RNA VirusesPositive-strand RNA viruses have genomes that function directly as messenger...

こちらも読む

関連記事

共著者、ジャーナル、引用グラフによってこの研究に関連する記事。

並び替え
Same author

Efficient use of longitudinal CD4 counts and viral load measures in survival analysis.

Statistics in medicine·2012
Same author

Virus entry via the alternative coreceptors CCR3 and FPRL1 differs by human immunodeficiency virus type 1 subtype.

Journal of virology·2009
Same author

A prospective study of risk factors for herpes simplex virus type 2 acquisition among high-risk HIV-1 seronegative women in Kenya.

Sexually transmitted infections·2009
Same author

Infants with late breast milk acquisition of HIV-1 generate interferon-gamma responses more rapidly than infants with early peripartum acquisition.

Clinical and experimental immunology·2009
Same author

Feline Pit2 functions as a receptor for subgroup B feline leukemia viruses.

Journal of virology·2001
Same author

Specificity in receptor usage by T-cell-tropic feline leukemia viruses: implications for the in vivo tropism of immunodeficiency-inducing variants.

Journal of virology·2001

関連する実験動画

Updated: Jun 22, 2026

Isolation of Fidelity Variants of RNA Viruses and Characterization of Virus Mutation Frequency
18:10

Isolation of Fidelity Variants of RNA Viruses and Characterization of Virus Mutation Frequency

Published on: June 16, 2011

選択力とレトロウイルス配列の変異に対する制約

J Overbaugh1, C R Bangham

  • 1Fred Hutchinson Cancer Research Center, Seattle, WA 98109, USA. joverbau@fhcrc.org

Science (New York, N.Y.)
|May 16, 2001
PubMed
まとめ

レトロウイルスは,誤りやすい逆転写酵素により急速に進化する. 免疫反応と標的細胞の利用可能性は,単なる変異ではなく,未治療の感染症におけるレトロウイルス多様性を駆動します.

科学分野:

  • ウイルス学 ウイルス学 ウイルス学
  • 進化生物学の進化生物学について
  • 免疫学 免疫学とは

背景:

  • レトロウイルスは,誤りやすい逆転写酵素による高変異率を示しています.
  • レトロウイルス配列の多様性と進化の程度は,異なるレトロウイルス種によって大きく異なります.

研究 の 目的:

  • レトロウイルス感染症における配列多様性と進化率の主要な要因を特定する.
  • レトロウイルスの遺伝子変異の形成における選択圧力の役割を調査する.

主な方法:

  • 様々なレトロウイルスにおける配列多様性の比較分析.
  • 選択力としての免疫応答と標的細胞の可用性の検討.
  • レンチウイルス (HIV,SIV) とオンコウイルス (FeLV,HTLV) を用いたケーススタディ.

主要な成果:

  • ウイルスの突然変異率は,多様性の唯一の制限要因ではありません; 選択は決定的です.
  • 免疫応答と限られた標的細胞の可用性は,重要な選択力である.
  • 選択圧力の差異は,観察された配列の多様性と疾患のアウトカムと相関しています.

結論:

さらに関連する動画

In Vitro Directed Evolution of a Restriction Endonuclease with More Stringent Specificity
09:16

In Vitro Directed Evolution of a Restriction Endonuclease with More Stringent Specificity

Published on: March 25, 2020

Reverse Genetics to Engineer Positive-Sense RNA Virus Variants
15:49

Reverse Genetics to Engineer Positive-Sense RNA Virus Variants

Published on: June 9, 2022

関連する実験動画

Last Updated: Jun 22, 2026

Isolation of Fidelity Variants of RNA Viruses and Characterization of Virus Mutation Frequency
18:10

Isolation of Fidelity Variants of RNA Viruses and Characterization of Virus Mutation Frequency

Published on: June 16, 2011

In Vitro Directed Evolution of a Restriction Endonuclease with More Stringent Specificity
09:16

In Vitro Directed Evolution of a Restriction Endonuclease with More Stringent Specificity

Published on: March 25, 2020

Reverse Genetics to Engineer Positive-Sense RNA Virus Variants
15:49

Reverse Genetics to Engineer Positive-Sense RNA Virus Variants

Published on: June 9, 2022

  • 選択,特に免疫圧力と宿主細胞の限界は,レトロウイルス多様性を決定する.
  • これらの力を理解することは,レトロウイルスの進化と疾患の進行を理解するために不可欠です.
  • 特定のレンチウイルスとオンコウイルスは,選択がウイルス集団をどのように形作るかを例示しています.