染色毒青的基因组组合为可转移元素的动态和基因组大小进化提供了洞察力
Carolin Dittrich1,2, Franz Hoelzl2, Steve Smith2
1Department of Biology and Environmental Sciences, University of Jyväskylä, Jyväskylä, Finland.
Genome biology and evolution
|May 16, 2024
概括
可转移元素通过在基因内核中积累,显著增加了染色毒青 (Dendrobates tinctorius) 的基因组大小. 这突出了它们在两动物基因组进化中的作用,并复杂了种群基因定型.
科学领域:
- 基因组学就是基因组学.
- 进化生物学 进化生物学
- 两动物研究研究
背景情况:
- 在整个生命中,基因组大小的变化是相当大的,可转移元素 (TE) 作为关键驱动因素.
- 两动物表现出极端的基因组大小多样性,使他们成为进化研究的宝贵模型.
- 高质量的两动物基因组组合在历史上一直很稀缺,限制了研究.
研究的目的:
- 为了生成染色毒青的高质量基因组组合,Dendrobates tinctorius.
- 研究可移植元素在驱动两动物基因组大小变异和基因大小演变中的作用.
- 评估TEs对D. tinctorius在人口层面的基因组分析的影响.
主要方法:
- 为Dendrobates tinctorius.生成一个高质量的基因组组件.
- 与其他可用的青基因组进行比较基因组分析,以确定合成和重组.
- 与基因特征 (内子) 相对应的可转移元素位置的量化和插入时间的分析.
- 人口规模移动元素测序以评估TE多样性和丰度.
主要成果:
- 成功生成了D. tinctorius的高质量基因组组.
- 进行比较时发现,在青谱系之间存在着保存的合成和显著的重组.
- 在基因组大小和基因大小之间发现了强烈的相关性,这是由 TE 在内子中的积累驱动的.
- 许多TE插入是最近出现的和特定于物种的,这复杂化了基因型化工作.
- TE的多样性和丰富性对使用重复元素的种群基因型定型构成了挑战.
结论:
- 可转移的元素对Dendrobates tinctorius的庞大基因组大小做出了重大贡献.
- 在两动物基因组中,TEs在塑造基因大小演变中发挥着至关重要的作用.
- 需要进一步的研究来理解TE动态,并优化重复基因组的基因型化策略.
相关概念视频
Overview of Transposition and Recombination
15.4K
Transposons make up a significant part of genomes of various organisms. Therefore, it is believed that transposition played a major evolutionary role in speciation by changing genome sizes and modifying gene expression patterns. For example, in bacteria, transposition can lead to conferring antibiotic resistance. Movement of transposable elements within the genetic pool of pathogenic bacteria can aid in transfer of antibiotic-resistant genetic elements. In eukaryotes, transposons can carry out...
15.4K
DNA-only Transposons
14.5K
DNA-only transposons are called autonomous transposons since they code for the enzyme transposase that is required for the transposition mechanism. Insertion of transposons can alter gene functions in multiple ways. They can mutate the gene, alter gene expression by introducing a novel promoter or insulator sequence, introduce new splice sites, and change the mRNA transcripts produced, or remodel chromatin structure.
The donor site from where the transposon is excised is either degraded or...
The donor site from where the transposon is excised is either degraded or...
14.5K
Exon Recombination
3.6K
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...
3.6K
LTR Retrotransposons
17.5K
LTR retrotransposons are class I transposable elements with long terminal repeats flanking an internal coding region. These elements are less abundant in mammals compared to other class I transposable elements. About 8 percent of human genomic DNA comprises LTR retrotransposons. Some of the common examples of LTR retrotransposons are Ty elements in yeast and Copia elements in Drosophila.
The internal coding region of LTR retrotransposons and their mechanism of transposition closely resembles a...
The internal coding region of LTR retrotransposons and their mechanism of transposition closely resembles a...
17.5K
Lampbrush Chromosomes
7.9K
In 1882, Flemming observed lampbrush chromosomes (LBC) in salamander eggs. Later in 1892, Rückert observed LBCs in shark egg cells and coined the term "lampbrush chromosomes" because they looked like brushes used to clean kerosene lamps.
LBCs are made up of two pairs of conjugating homologous chromatids. Each chromatid consists of alternatively positioned regions of condensed-inactive chromatin and loosely placed-active side loops, which can be contracted and extended. The loops...
LBCs are made up of two pairs of conjugating homologous chromatids. Each chromatid consists of alternatively positioned regions of condensed-inactive chromatin and loosely placed-active side loops, which can be contracted and extended. The loops...
7.9K
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


