染色体和人类疾病:拼接破碎过程的碎片
Christopher A Maher1, Richard K Wilson
1The Genome Institute, Washington University School of Medicine, St. Louis, MO 63108, USA. cmaher@dom.wustl.edu
Cell
|January 24, 2012
概括
高通量基因组学揭示了染色体,这是一个基因组区域在一次事件中破碎并重新连接的过程. 了解其机制是研究发育和疾病中的基因组重组的关键.
科学领域:
- 基因组学就是基因组学.
- 分子生物学分子生物学
- 遗传学 是一个遗传学.
背景情况:
- 高通量基因组学为研究基因组事件提供了前所未有的分辨率.
- 最近发现了染色体,这是一种涉及基因组破碎和重聚的现象.
- 基因组重组在生物发育和疾病发病过程中起着至关重要的作用.
研究的目的:
- 总结一下对染色体的新兴理解.
- 探索潜在的背后的染色体的潜在机制.
- 讨论染色体对于发育和疾病的影响.
主要方法:
- 审查最近的高通量基因组学研究.
- 对染色体的新兴机械模型的分析.
- 综合有关基因组重组的当前知识.
主要成果:
- 染色体的特点是特定的基因组区域的破碎和随后的重聚.
- 新兴研究正在开始阐明推动这种复杂的基因组重组的潜在机制.
- 这种现象对理解遗传疾病和发育过程有重大影响.
结论:
- 染色体形代表了基因组不稳定性的重大发现.
- 对染色体变机制的进一步研究对于推动我们对基因组稳定性的理解至关重要.
- 这种现象为大规模基因组重组在疾病病因学中的作用提供了新的见解.
相关概念视频
Mutations
98.2K
Overview
98.2K
Gene Conversion
10.9K
Other than maintaining genome stability via DNA repair, homologous recombination plays an important role in diversifying the genome. In fact, the recombination of sequences forms the molecular basis of genomic evolution. Random and non-random permutations of genomic sequences create a library of new amalgamated sequences. These newly formed genomes can determine the fitness and survival of cells. In bacteria, homologous and non-homologous types of recombination lead to the evolution of new...
10.9K
Genomic Imprinting and Inheritance
38.9K
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...
The expression of some genes depends on which parent passed the gene to the offspring, through a phenomenon known as...
38.9K
Genome Copying Errors
5.6K
DNA replication is a well-evolved process that copies millions of base pairs with high fidelity during each cell division. Occasionally a wrong base or a long stretch of wrong bases may get added to the daughter strands. If the errors are left unchecked, cells might accumulate several mutations that might endanger their survival. Therefore, the copying errors are checked and repaired at three levels.
5.6K
Exon Recombination
4.3K
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...
Exon shuffling follows “splice frame rules.” Each exon...
4.3K
Mutations
45.8K
Mutations are changes in the sequence of DNA. These changes can occur spontaneously or they can be induced by exposure to environmental factors. Mutations can be characterized in a number of different ways: whether and how they alter the amino acid sequence of the protein, whether they occur over a small or large area of DNA, and whether they occur in somatic cells or germline cells.
Chromosomal Alterations Are Large-Scale Mutations
While point mutations are changes in a single nucleotide in...
Chromosomal Alterations Are Large-Scale Mutations
While point mutations are changes in a single nucleotide in...
45.8K


