在人类基因的编码区域中,C和G经常突变为T和A
1School of Food and Biological Engineering, Jiangsu University, 301 Xuefu Road, Zhenjiang, 212013, China. ywang@ujs.edu.cn.
Molecular genetics and genomics : MGG
|March 2, 2024
概括
人类基因突变,特别是C / G到T / A的变化,是由需要减少DNA键和基因表达期间的能量消耗驱动的. 这种进化趋势影响了疾病的发生和健康挑战.
科学领域:
- 遗传学 是一个遗传学.
- 分子生物学分子生物学
- 进化生物学 进化生物学
背景情况:
- 人类基因中的核酸突变与严重疾病有关.
- 了解突变模式和进化趋势对于人类健康至关重要.
研究的目的:
- 在人类基因中统计分析单核酸变异 (SNVs).
- 根据突变模式推断人类基因的进化趋势.
主要方法:
- 统计分析了18339个人类基因的编码区域中的89895个SNV.
- 检查突变类型及其与DNA结构和能量消耗的相关性.
主要成果:
- 在人类基因中,C/G到T/A突变很常见,可减少键.
- 这种减少降低了DNA复制,转录和mRNA翻译的能量需求.
- 代突变频率与代含量相关,表明减少键的驱动力.
结论:
- 减少键是人类核酸突变的重要驱动力.
- 突变主要旨在减少基因表达中的能量消耗,而不是改变特定的氨基酸.
- 这项研究提供了一个模型,可以使用其他生物体中的SNV数据推断进化趋势.
相关概念视频
Genome Copying Errors
4.2K
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.
4.2K
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
Mutations
37.3K
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...
37.3K
Proofreading
54.1K
Overview
54.1K
Gene Conversion
9.8K
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...
9.8K
RNA Editing
9.0K
RNA editing is a post-transcriptional modification where a precursor mRNA (pre-mRNA) nucleotide sequence is changed by base insertion, deletion, or modification. The extent of RNA editing varies from a few hundred bases, in mitochondrial DNA of trypanosomes, to a just single base, in nuclear genes of mammals. Even a single base change in the pre-mRNA can convert a codon for one amino acid into the codon for another amino acid or a stop codon. This type of re-coding can significantly affect the...
9.0K


