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関連する概念動画

Pleiotropy01:33

Pleiotropy

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Pleiotropy is the phenomenon in which a single gene impacts multiple, seemingly unrelated phenotypic traits. For example, defects in the SOX10 gene cause Waardenburg Syndrome Type 4, or WS4, which can cause defects in pigmentation, hearing impairments, and an absence of intestinal contractions necessary for elimination. This diversity of phenotypes results from the expression pattern of SOX10 in early embryonic and fetal development. SOX10 is found in neural crest cells that form melanocytes,...
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Epistasis01:39

Epistasis

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In addition to multiple alleles at the same locus influencing traits, numerous genes or alleles at different locations may interact and influence phenotypes in a phenomenon called epistasis. For example, rabbit fur can be black or brown depending on whether the animal is homozygous dominant or heterozygous at a TYRP1 locus. However, if the rabbit is also homozygous recessive at a locus on the tyrosinase gene (TYR), it will have an unshaded coat that appears white, regardless of its TYRP1...
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Regulation of the Unfolded Protein Response01:31

Regulation of the Unfolded Protein Response

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Inositol-requiring kinase one or IRE1 is the most conserved eukaryotic unfolded protein response (UPR) receptor. It is a type I transmembrane protein kinase receptor with a distinctive site-specific RNase activity. As the binding mechanics of the misfolded proteins with the N-terminal domain of IRE-1 are unclear, three binding models — direct, indirect, and allosteric -- are proposed for receptor activation. Nevertheless, it is known that once a misfolded protein associates with IRE1, it...
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Exon Recombination02:32

Exon Recombination

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The evolution of new genes is critical for speciation. Exon recombination, also known as exon shuffling or domain shuffling, is an important means of new gene formation. It is observed across vertebrates, invertebrates, and in some plants such as potatoes and sunflowers. During exon recombination, exons from the same or different genes recombine and produce new exon-intron combinations, which might evolve into new genes. 
Exon shuffling follows “splice frame rules.” Each exon...
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Epistasis Analysis01:09

Epistasis Analysis

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Although Mendel chose seven unrelated traits in peas to study gene segregation, most traits involve multiple gene interactions that create a spectrum of phenotypes. When the interaction of various genes or alleles at different locations influences a phenotype, this is called epistasis. Epistasis often involves one gene masking or interfering with the expression of another (antagonistic epistasis). Epistasis often occurs when different genes are part of the same biochemical pathway. The...
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Position-effect Variegation02:32

Position-effect Variegation

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In 1928, a German botanist Emil Heitz observed the moss nuclei with a DNA binding dye. He observed that while some chromatin regions decondense and spread out in the interphase nucleus, others do not. He termed them euchromatin and heterochromatin, respectively. He proposed that the heterochromatin regions reflect a functionally inactive state of the genome. It was later confirmed that heterochromatin is transcriptionally repressed, and euchromatin is transcriptionally active chromatin.
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このページは機械翻訳されています。他のページは英語で表示される場合があります。View in English
  1. ホーム
  2. 研究分野
  3. 生物学的科学
  4. 遺伝学
  5. エピジェネティクス (ゲノムメチレーションとエピジェノミクスを含む)
  6. 広範囲のプレオトロピズムとアレル異質性は,irx3とirx5の代謝効果を媒介する.

広範囲のプレオトロピズムとアレル異質性は,IRX3とIRX5の代謝効果を媒介する.

Débora R Sobreira1, Amelia C Joslin2, Qi Zhang2,3

  • 1Department of Human Genetics, University of Chicago, Chicago, IL 60637, USA. deborarsobreira@gmail.com ianeas@bsd.uchicago.edu nobrega@uchicago.edu.

Science (New York, N.Y.)
|June 4, 2021

関連する実験動画

Electrophoretic Mobility Shift Assay EMSA for the Study of RNA-Protein Interactions: The IRE/IRP Example
12:44

Electrophoretic Mobility Shift Assay EMSA for the Study of RNA-Protein Interactions: The IRE/IRP Example

Published on: December 3, 2014

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A Non-random Mouse Model for Pharmacological Reactivation of Mecp2 on the Inactive X Chromosome
08:27

A Non-random Mouse Model for Pharmacological Reactivation of Mecp2 on the Inactive X Chromosome

Published on: May 22, 2019

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Ubiquitous and Tissue-specific RNA Targeting in Drosophila Melanogaster using CRISPR/CasRx
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Ubiquitous and Tissue-specific RNA Targeting in Drosophila Melanogaster using CRISPR/CasRx

Published on: February 5, 2021

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PubMed で要約を見る

まとめ
この要約は機械生成です。

FTO遺伝子の近くの遺伝子変異は,IRX3とIRX5の遺伝子発現を調節することによって,肥満のリスクに影響します. これらの非コード変異は複数の組織に影響し,一時的に制限された効果を持ち,疾患リスクの複雑な遺伝構造を明らかにします.

科学分野:

  • 遺伝学
  • ゲノミクス
  • 分子生物学

背景:

  • ノンコーディング変種は特定の組織と時間枠における遺伝子発現を制御する.
  • FTO遺伝子領域は 肥満のリスクと強く関連しています
  • 複雑な病気の遺伝子を解読するには 規制変異を理解することが重要です

研究 の 目的:

  • 肥満に関連するFTOゲノム領域の遺伝的・機能的構造を調査する.
  • この領域の変異が遺伝子発現と現象的結果にどのように影響するか判断する.
  • 非コード化変異のプレオトロピクおよび時間的に制限された効果を調査する.

主な方法:

  • FTO遺伝子領域内の遺伝子変異の分析
  • IRX3とIRX5を標的とする強化剤の機能的特徴
  • 複数の組織と時間窓における遺伝子発現の評価

主要な成果:

  • 共通のハプロタイプの複数の変異は,メガベース距離からIRX3とIRX5を標的とした増強剤の活性を変化させる.
  • これらの増強剤は脂肪組織と脳における遺伝子発現を調節する.
  • 規制効果は限られた時間枠で観察された.

関連する実験動画

Electrophoretic Mobility Shift Assay EMSA for the Study of RNA-Protein Interactions: The IRE/IRP Example
12:44

Electrophoretic Mobility Shift Assay EMSA for the Study of RNA-Protein Interactions: The IRE/IRP Example

Published on: December 3, 2014

54.2K
A Non-random Mouse Model for Pharmacological Reactivation of Mecp2 on the Inactive X Chromosome
08:27

A Non-random Mouse Model for Pharmacological Reactivation of Mecp2 on the Inactive X Chromosome

Published on: May 22, 2019

6.5K
Ubiquitous and Tissue-specific RNA Targeting in Drosophila Melanogaster using CRISPR/CasRx
06:37

Ubiquitous and Tissue-specific RNA Targeting in Drosophila Melanogaster using CRISPR/CasRx

Published on: February 5, 2021

3.3K

結論:

  • 肥満リスクロシウムの遺伝的構造には,広範囲のプレオトロピーとアレルの異質性が含まれています.
  • 組織全体に共通するアレル効果と,一時的に制限された規制効果は,重要な特徴です.
  • ノンコーディング変種は,疾患の病因学において複雑で多面的な役割を果たすことができます.