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Karyotyping01:17

Karyotyping

Describing the number and physical features of chromosomes can reveal abnormalities that underlie genetic diseases. This description is facilitated by special staining techniques that produce a particular banding pattern on each chromosome. State-of-the-art techniques make this approach even more powerful, enabling the detection of individual genes that cause disease.A Simple Chromosome Staining Technique Provides Valuable Scientific InsightSome genetic diseases can be detected by looking at...
Genomic Imprinting and Inheritance02:30

Genomic Imprinting and Inheritance

Diploid organisms inherit genetic material through chromosomes from both parents. Copies of the same gene are known as alleles. In most cases, both alleles are simultaneously expressed and allow various cellular processes to function optimally. If one of the alleles is missing or mutated, the expression of the other allele can compensate; however, this is not true for all genes.
The expression of some genes depends on which parent passed the gene to the offspring, through a phenomenon known as...
Meiosis vs. Mitosis02:57

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...
Nondisjunction01:21

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...
Teratogenicity01:07

Teratogenicity

The ability of a drug to produce structural deformations and functional abnormalities in the developing embryo or the fetus is called teratogenicity, and the drug producing this effect is known as a teratogen. Teratogenic effects include stillbirth, miscarriage, intrauterine growth restriction, and neurocognitive delay. A teratogen may affect the embryo at different stages of development, which is important in determining the type and extent of the damage. During blastocyst formation, the early...

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Updated: Jul 8, 2026

Assessing Teratogenic Changes in a Zebrafish Model of Fetal Alcohol Exposure
10:07

Assessing Teratogenic Changes in a Zebrafish Model of Fetal Alcohol Exposure

Published on: March 20, 2012

胚のエピジェネティック欠陥の幹細胞の結果

Cinzia Allegrucci1, Chris Denning, Helen Priddle

  • 1Division of Obstetrics and Gynaecology, University of Nottingham, Queens Medical Centre, Nottingham NG7 2UH, UK.

Lancet (London, England)
|July 13, 2004
PubMed
まとめ

初期の発達における表皮遺伝的再プログラミングは,遺伝子発現と細胞の分化に不可欠である. 卵細胞のメカニズムの理解は,体細胞の再プログラムを改善し,胚性幹細胞技術におけるエラーを回避することができます.

科学分野:

  • エピジェネティクスと発達生物学
  • 幹細胞生物学 幹細胞生物学
  • ゲノムインプリントング (Genomic Imprinting) とは

背景:

  • ソマティック細胞は,すべてのタンパク質の遺伝コードを持っているが,表遺伝的改変は,系統特異的な遺伝子発現を調節する.
  • ヒストンとDNAの改変 (アセチル化,メチル化) はクロマチンの構造を変化させ,遺伝子活動を制御する.
  • 受精後,精子のプロタミンは卵細胞ヒストンに取って代わられ,胚のゲノム再プログラムを開始します.

研究 の 目的:

  • 卵細胞における表遺伝的再プログラムメカニズムと,体細胞の再プログラムの可能性を調査する.
  • 胚技術におけるエピジェネティックエラーが幹細胞の性質に及ぼす影響を調査する.
  • ソマティック細胞核移転 (SCNT) での表遺伝的エラーを回避するための戦略を特定する.

主な方法:

  • 人間の胚性幹細胞の誘導と哺乳類の胚技術に関する最近の研究のレビュー.
  • 卵細胞と初期の胚における表遺伝的再プログラミングプロセスの分析.
  • 精子と体細胞クロマチンの状態の比較分析.

主要な成果:

  • 人間の胚性幹細胞系は,治療用クローニングと超数の胚から得られている.

さらに関連する動画

Generation of Induced Pluripotent Stem Cells from Turner Syndrome (45XO) Fetal Cells for Downstream Modelling of Neurological Deficits Associated with the Syndrome
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Generation of Induced Pluripotent Stem Cells from Turner Syndrome (45XO) Fetal Cells for Downstream Modelling of Neurological Deficits Associated with the Syndrome

Published on: December 4, 2021

Chromosome Screening of Human Preimplantation Embryos by Using Spent Culture Medium: Sample Collection and Chromosomal Ploidy Analysis
12:32

Chromosome Screening of Human Preimplantation Embryos by Using Spent Culture Medium: Sample Collection and Chromosomal Ploidy Analysis

Published on: September 7, 2021

関連する実験動画

Last Updated: Jul 8, 2026

Assessing Teratogenic Changes in a Zebrafish Model of Fetal Alcohol Exposure
10:07

Assessing Teratogenic Changes in a Zebrafish Model of Fetal Alcohol Exposure

Published on: March 20, 2012

Generation of Induced Pluripotent Stem Cells from Turner Syndrome (45XO) Fetal Cells for Downstream Modelling of Neurological Deficits Associated with the Syndrome
09:39

Generation of Induced Pluripotent Stem Cells from Turner Syndrome (45XO) Fetal Cells for Downstream Modelling of Neurological Deficits Associated with the Syndrome

Published on: December 4, 2021

Chromosome Screening of Human Preimplantation Embryos by Using Spent Culture Medium: Sample Collection and Chromosomal Ploidy Analysis
12:32

Chromosome Screening of Human Preimplantation Embryos by Using Spent Culture Medium: Sample Collection and Chromosomal Ploidy Analysis

Published on: September 7, 2021

  • 哺乳類の胚技術では,潜在的に幹細胞の特性に影響を与える,表遺伝的エラーの傾向を示しています.
  • 卵細胞は精子ゲノムを再プログラムする固有のメカニズムを有しており,標的の表遺伝子操作のモデルを提供しています.
  • 結論:

    • 卵細胞の再プログラムメカニズムを特定することで,SCNTを回避して体細胞のインビトロ再プログラムが可能になる.
    • ターゲットを絞ったエピジェネティックアプローチは,現在のSCNT方法に関連するエラーを回避することができます.
    • ヒトの胚性幹細胞に表遺伝的エラーが及ぼす影響を明らかにするために,さらなる研究が必要である.