转位子编码的内核与导向RNA之间的对抗性冲突
Rimantė Žedaveinytė1, Chance Meers1, Hoang C Le1
1Department of Biochemistry and Molecular Biophysics, Columbia University, New York, NY 10032, USA.
概括
这项研究揭示了IS607家族转子,编码I组内子,如何平衡RNA活动的自我扩散. 这些元素控制结合产物和指导RNA,确保转体子传播,同时最大限度地减少宿主损害.
科学领域:
- 分子生物学
- 遗传学
- 微生物学
背景情况:
- TnpB核酶是CRISPR-Cas12酶的进化前体.
- IS605家族的TnpB同源体作为RNA引导的内核酶,对通过同源重组维持转子体至关重要.
研究的目的:
- 阐明IS607家族元素的转换生命周期机制.
- 在特定元素 ("IStron") 中确定规范其活动的特征.
主要方法:
- 对IS607家族元素的转换生命周期的分析
- 来自Clostridium botulinum的"IStron"中的特定分子特征的识别
主要成果:
- 发现了控制IS607家族元素转移的分子机制.
- 在"IStron"中确定了控制结合产品和指导RNA之间的平衡的调节特征.
- 证明IStron转录平衡竞争活动以促进转子传播和限制宿主健康成本.
结论:
- 转子编码的非编码RNA具有多功能功用.
- IS607家族元素具有进化的机制来平衡自私的传播与宿主健康.
- 这项工作突显了转子编码非编码RNA的分子创新.
相关概念视频
RNA Interference
26.0K
RNA interference (RNAi) is a process in which a small non-coding RNA molecule blocks the post-transcriptional expression of a gene by binding to its messenger RNA (mRNA) and preventing the protein from being translated.
This process occurs naturally in cells, often through the activity of genomically-encoded microRNAs. Researchers can take advantage of this mechanism by introducing synthetic RNAs to deactivate specific genes for research or therapeutic purposes. For example, RNAi could be used...
This process occurs naturally in cells, often through the activity of genomically-encoded microRNAs. Researchers can take advantage of this mechanism by introducing synthetic RNAs to deactivate specific genes for research or therapeutic purposes. For example, RNAi could be used...
26.0K
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
RNA Splicing
56.3K
Splicing is the process by which eukaryotic RNA is edited before its translation into protein. The RNA strand transcribed from eukaryotic DNA is called the primary transcript. The primary transcripts that become mRNAs are called precursor messenger RNAs (pre-mRNAs). Eukaryotic pre-mRNA contains alternating sequences of exons and introns. Exons are nucleotide sequences that code for proteins, whereas introns are the non-coding regions. In RNA splicing, introns are removed and exons are bonded...
56.3K
piRNA - Piwi-interacting RNAs
6.8K
PIWI-interacting RNAs, or piRNAs, are the most abundant short non-coding RNAs. More than 20,000 genes have been found in humans that code for piRNAs while only 2000 genes have been found for miRNAs. piRNAs can act at the transcriptional and post-transcriptional levels and have a vital role in silencing transposable elements present in germ cells. They are also involved in epigenetic silencing and activation. Previously, they were thought to function only in germ cells but new evidence suggests...
6.8K
siRNA - Small Interfering RNAs
16.7K
Small interfering RNAs, or siRNAs, are short regulatory RNA molecules that can silence genes post-transcriptionally, as well as the transcriptional level in some cases. siRNAs are important for protecting cells against viral infections and silencing transposable genetic elements.
In the cytoplasm, siRNA is processed from a double-stranded RNA, which comes from either endogenous DNA transcription or exogenous sources like a virus. This double-stranded RNA is then cleaved by the...
In the cytoplasm, siRNA is processed from a double-stranded RNA, which comes from either endogenous DNA transcription or exogenous sources like a virus. This double-stranded RNA is then cleaved by the...
16.7K
DNA-only Transposons
14.4K
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...
14.4K


