人类类特有的可移植元素在面发育过程中重塑了神经的迁移.
Laura Deelen1, Zoe H Mitchell1, Martina Demurtas1
1Department of Life Sciences, Imperial College London, SW7 2AZ, London, UK.
Molecular systems biology
|September 22, 2025
概括
新进化的可转移元素在人类头骨神经细胞中充当增强剂,影响头骨面部发育和进化. 抑制这些元素会损害细胞迁移,改变基因表达.
科学领域:
- 进化生物学是进化的生物学.
- 基因组学就是基因组学.
- 发育生物学是发展生物学.
背景情况:
- 面发育对于脊椎动物的进化至关重要,由于调节网络的变化,产生了特定物种的特征.
- 可转移元素 (TE) 驱动基因组进化,但它们在神经细胞 (CNCC) 中的特定作用尚不清楚.
研究的目的:
- 研究人类CNCC规范中作为增强剂的类人特异性TE (LTR5Hs和SVA) 的化.
- 确定这些TE对面发育和进化的影响.
主要方法:
- 使用人类诱导的多能干细胞 (iPSC) 衍生的CNCCs.
- 通过CRISPR干扰,确定了作为增强剂起作用的同类动物特异性TE.
- 进行了转录分析和功能分析,以评估CNCC迁移和基因表达.
主要成果:
- 发现了约515种类型特异性TEs作为人类CNCC的增强剂,其中约250种是人类特异性 (主要是LTR5Hs).
- 这些TEs以CNCC图案进行丰富,由TWIST1结合,并表现出CNCC特有的增强剂活性.
- 这些TEs的抑制破坏了基因表达,损害了CNCC迁移,与黑猩猩相比,使人类特异性基因表达差异正常化.
结论:
- 年轻的TE已经被化,以调节CNCC,微调发展网络.
- 这种TE化可能有助于人类的特定血统的面进化.
相关概念视频
Non-LTR Retrotransposons
13.2K
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...
13.2K
Overview of Transposition and Recombination
18.8K
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...
18.8K
Determination
20.8K
During embryogenesis, cells become progressively committed to different fates through a two-step process: specification followed by determination. Specification is demonstrated by removing a segment of an early embryo, “neutrally” culturing the tissue in vitro—for example, in a petri dish with simple medium—and then observing the derivatives. If the cultured region gives rise to cell types that it would normally generate in the embryo, this means that it is specified. In...
20.8K
Neurulation
45.4K
Neurulation is the embryological process which forms the precursors of the central nervous system and occurs after gastrulation has established the three primary cell layers of the embryo: ectoderm, mesoderm, and endoderm. In humans, the majority of this system is formed via primary neurulation, in which the central portion of the ectoderm—originally appearing as a flat sheet of cells—folds upwards and inwards, sealing off to form a hollow neural tube. As development proceeds, the...
45.4K
LTR Retrotransposons
19.5K
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...
19.5K
DNA-only Transposons
17.2K
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...
17.2K


