在发现和分析人类双重重复的进步
Mark J P Chaisson1,2, Arvis Sulovari3, Paul N Valdmanis4,5,6
1Department of Quantitative and Computational Biology, University of Southern California, Los Angeles, CA 90089, U.S.A.
Emerging topics in life sciences
|October 31, 2023
概括
长读测序揭示了人类基因组中并联重复的DNA的复杂结构. 了解这种变异对于诊断和治疗遗传疾病至关重要.
科学领域:
- 基因组学就是基因组学.
- 人类遗传学 人类遗传学
- 分子生物学分子生物学
背景情况:
- 串联重复的DNA,包括短串联重复 (STR) 和卫星阵列,构成了人类基因组的很大一部分.
- 从历史上看,由于这些区域的重复性,分析这些区域一直是具有挑战性的.
- 长读测序的进步为研究这些复杂的基因组区域提供了新的可能性.
研究的目的:
- 审查当前对人类基因组中协同重复的DNA组织的理解.
- 突出这些地区在人类疾病中的重要性.
- 讨论分析它们的遗传多样性和功能影响的进展和挑战.
主要方法:
- 对长时间阅读测序技术的现有文献的审查.
- 对可视化和解释重复模式的计算方法的分析.
- 整合有关遗传变异,疾病关联,基因表达和表观遗传学的数据.
主要成果:
- 长读序列提供了前所未有的访问结构和组合的所有类别的协同重复的DNA.
- 新的计算方法正在出现,以分析这些区域内人类变异的复杂模式.
- 这些模式与疾病,基因表达和表观遗传修饰有关.
结论:
- 对重复丰富变异的准确表征对人类遗传学变得越来越重要.
- 这种理解将影响基础研究和临床应用.
- 未来的研究很可能会关注重复变化的功能后果.
相关概念视频
Next-generation Sequencing
89.0K
The first human genome sequencing project cost $2.7 billion and was declared complete in 2003, after 15 years of international cooperation and collaboration between several research teams and funding agencies. Today, with the advent of next-generation sequencing technologies, the cost and time of sequencing a human genome have dropped over 100 fold.
Next-Generation Sequencing Methods
Although all next-generation methods use different technologies, they all share a set of standard features....
Next-Generation Sequencing Methods
Although all next-generation methods use different technologies, they all share a set of standard features....
89.0K
Peptide Identification Using Tandem Mass Spectrometry
6.5K
Tandem mass spectrometry, also known as MS/MS or MS2, is an analytical technique that employs two mass analyzers. Essentially it is a series of mass spectrometers that helps isolate a particular biomolecule and then helps study its chemical properties.
This technique helps gather information regarding the protein from which the peptide was obtained and to study the peptides’ amino acid sequence. Identifying peptides from a complex mixture is an important component of the growing field of...
This technique helps gather information regarding the protein from which the peptide was obtained and to study the peptides’ amino acid sequence. Identifying peptides from a complex mixture is an important component of the growing field of...
6.5K
Comparing Copy Number Variations and SNPs
17.7K
Sequencing of the human genome has opened up several best-kept secrets of the genome. Scientists have identified thousands of genome variations that exist within a population. These variations can be a single nucleotide or a larger chromosomal variation.
Copy number variations or CNVs are the structural variations that cover more than 1kb of DNA sequence. The single nucleotide polymorphism (SNP), on the other hand, is a single nucleotide change or a point mutation that is found in more than 1%...
Copy number variations or CNVs are the structural variations that cover more than 1kb of DNA sequence. The single nucleotide polymorphism (SNP), on the other hand, is a single nucleotide change or a point mutation that is found in more than 1%...
17.7K
Sanger Sequencing
754.6K
DNA sequencing is a fundamental technique that is routinely used in the biological sciences. This method can be applied to a range of questions at different scales - from the sequencing of a cloned DNA fragment or the study of a mutation in a gene up to whole-genome sequencing. However, despite the widespread use of sequencing today, it was not until 1977 that Fredrick Sanger and his collaborators developed the chain-termination method to decode DNA sequences. It relies on the separation of a...
754.6K
Non-LTR Retrotransposons
11.5K
As the name suggests, non-LTR retrotransposons lack the long terminal repeats characteristic of the LTR retrotransposons. Additionally, both LTR and non-LTR retrotransposons use distinct mechanisms of mobilization. Non-LTR retrotransposons are further divided into two classes - Long interspersed nuclear elements (LINEs) and short interspersed nuclear elements (SINEs), both of which occur abundantly in most mammals, including humans. Some of the active non-LTR retrotransposons in humans are L1...
11.5K
Gene Duplication and Divergence
6.1K
The seminal work of Ohno in 1970 popularized the idea of gene duplication and divergence. DNA sequence comparison studies reveal that a large portion of the genes in bacteria, archaebacteria, and eukaryotes was generated by gene duplication and divergence, indicating its critical role in evolution.
The duplicated copies of the gene are called Paralogs. Paralogs with similar sequences and functions form a gene family. Across several species, a large number of gene families are...
The duplicated copies of the gene are called Paralogs. Paralogs with similar sequences and functions form a gene family. Across several species, a large number of gene families are...
6.1K


