関連する実験動画
Updated: Jul 14, 2026

09:16
Meiotic Spindle Assessment in Mouse Oocytes by siRNA-mediated Silencing
Published on: October 11, 2015
オリゴシンダクティリー (Oligosyndactyly):マウスの致命的な変異で,発達の非常に早い段階でミトの停止を引き起こす
Cell
|October 1, 1984
まとめ
オリゴシンダクティリー (Os) 変異は,ミトーシス中の細胞を停止することによって,同卵性マウスの発達の致死性を引き起こします. このユニークな突然変異は,正常なミトスのスパインドルにもかかわらず,メタフェーズプレートから染色体の移動を妨げます.
科学分野:
- 発達生物学 発達生物学とは
- 遺伝学 遺伝学とは
- 細胞生物学 細胞生物学
背景:
- マウスのオリゴシンダクティリー (Os) 変異は,ヘテロジゴトのシンダクティリー,筋肉異常,糖尿病インシピドゥスを引き起こします.
- ホモジゴス Os変異は,胚の発達初期に致命的です.
研究 の 目的:
- ホモジゴス Os 変異の致死性の基礎となる分子機構を定義する.
- 同卵性オスの胚におけるミトス欠陥の性質を特徴づけるために.
主な方法:
- ブラストキスト段階における同胞胚の分析.
- ミトスのスパインドルと染色体行動の細胞学的検査.
主要な成果:
- ホモジゴス胚は,細胞が芽細胞段階でのミトーシスに蓄積され停止する.
- ミトスのは正常に見えますが,染色体はメタフェーズプレートから移動することができません.
- これは,染色体分離の特定の欠陥を引き起こす最初の定義された哺乳類の発達変異を表しています.
結論:
- Os変異は,同卵性状態では,ミトーシス中の染色体分離を妨げます.
- この欠陥は,より高い真核生物における既知のミトス停止変異の中でユニークである.
- Osは,染色体運動と発達的致死性を研究するための新しいモデルを提供します.
関連する概念動画
In-vitro Mutagenesis
To learn more about the function of a gene, researchers can observe what happens when the gene is inactivated or “knocked out,” by creating genetically engineered knockout animals. Knockout mice have been particularly useful as models for human diseases such as cancer, Parkinson’s disease, and diabetes.
Nondisjunction
During meiosis, chromosomes occasionally separate improperly. This occurs due to failure of homologous chromosome separation during meiosis I or failed sister chromatid separation during meiosis II. In some species, notably plants, nondisjunction can result in an organism with an entire additional set of chromosomes, which is called polyploidy. In humans, nondisjunction can occur during male or female gametogenesis and the resulting gametes possess one too many or one too few chromosomes.
Lethal Alleles
Agouti: A Lethal Allele
Lucien Cuénot discovered lethal alleles in 1905 while studying the inheritance of coat color in mice. The agouti gene is responsible for the color of the coat in mice. This gene codes for an agouti-signaling protein, which is responsible for melanin distribution in mammals. The wild-type allele gives rise to gray-brown coat color in mice, while the mutant allele gives rise to yellow coat color. In addition to coat color, the agouti gene is associated with the yellow...
Lucien Cuénot discovered lethal alleles in 1905 while studying the inheritance of coat color in mice. The agouti gene is responsible for the color of the coat in mice. This gene codes for an agouti-signaling protein, which is responsible for melanin distribution in mammals. The wild-type allele gives rise to gray-brown coat color in mice, while the mutant allele gives rise to yellow coat color. In addition to coat color, the agouti gene is associated with the yellow...
Meiosis II
Meiosis II entails cell division and segregation of the sister chromatids, resulting in the production of four unique haploid gametes. The steps for meiosis II are similar to mitosis, except that meiosis II occurs in haploid cells, whereas mitosis occurs in diploid cells.
The timing and cell division patterns of meiosis differ between males and females. In male meiosis, the centrosomes are part of the formation of the meiotic spindle. However, in oocytes, including that of humans, Drosophila,...
The timing and cell division patterns of meiosis differ between males and females. In male meiosis, the centrosomes are part of the formation of the meiotic spindle. However, in oocytes, including that of humans, Drosophila,...
Meiosis vs. Mitosis
Cell division is necessary for growth and reproduction in organisms. Mitosis aids cell growth and development by dividing somatic cells. In contrast, meiosis causes the division of germ cells and plays an essential role in sexual reproduction. Due to their unique functional requirements, mitosis and meiosis differ from each other in multiple aspects.
Before the start of mitosis and meiosis I, the cell synthesizes DNA, resulting in two homologous copies of each chromosome. DNA synthesis is...
Before the start of mitosis and meiosis I, the cell synthesizes DNA, resulting in two homologous copies of each chromosome. DNA synthesis is...
Nondisjunction
Nondisjunction is the failure of homologous chromosomes or sister chromatids to separate correctly and move to the opposite poles of the cells. This produces daughter cells with abnormal chromosome numbers. Nondisjunction is common during anaphase I or anaphase II of meiosis. Mutations in synaptonemal complex proteins that attach homologous chromosomes increase the chances of nondisjunction in anaphase I of meiosis I. In contrast, mutations in topoisomerases and condensins that hold sister...

