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相关概念视频

siRNA - Small Interfering RNAs02:30

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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.
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RNA Interference01:23

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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.
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RNA Splicing01:32

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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...
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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...
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RNA interference (RNAi) is a cellular mechanism that inhibits gene expression by suppressing its transcription or activating the RNA degradation process. The mechanism was discovered by Andrew Fire and Craig Mello in 1998 in plants. Today, it is observed in almost all eukaryotes, including protozoa, flies, nematodes, insects, parasites, and mammals. This precise cellular mechanism of gene silencing has been developed into a technique that provides an efficient way to identify and determine the...
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A gene is a stretch of DNA that serves as the blueprint for functional RNAs and proteins. Since DNA is comprised  of nucleotides and proteins are comprised of amino acids, a mediator is required to convert the information encoded in DNA into proteins. This mediator is the messenger RNA (mRNA). mRNA copies the blueprint from DNA by a process called transcription. In eukaryotes, transcription occurs in the nucleus by complementary base-pairing with the DNA template. The mRNA is then...
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Cell Based Assays of SINEUP Non-coding RNAs That Can Specifically Enhance mRNA Translation
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如何反意义转录可以进化为编码新型蛋白质.

Bharat Ravi Iyengar1, Anna Grandchamp2,3, Erich Bornberg-Bauer2,4

  • 1Institute for Evolution and Biodiversity, University of Münster, Hüfferstrasse 1, Münster, Germany. b.ravi@uni-muenster.de.

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此摘要是机器生成的。

新的蛋白质编码基因可以从非编码RNA中产生. 与现有基因的反意义重叠促进了这些新的开放阅读框架 (ORF) 的出现和保留,特别是在特定的阅读框架中.

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科学领域:

  • 进化基因组学是进化的基因组学.
  • 分子进化是分子进化的过程.
  • RNA生物学的RNA生物学

背景情况:

  • 蛋白质编码特征可以在非编码转录中出现de novo,从而导致新的蛋白质编码基因.
  • 跨物种的大量新型非编码RNA表现出与蛋白质编码基因的反意义重叠.
  • 这些反意义RNA中的开放读取框架 (ORF) 可能与现有的ORF重叠.

研究的目的:

  • 调查ORF进化的进化约束,因为在三个读取框架中与现有的ORF重叠.
  • 确定反意义重叠如何影响ORF的出现和丧失.

主要方法:

  • 数学建模的组合. 数学建模的组合.
  • 在两个模型生物体中对基因组和转录组数据进行分析.

主要成果:

  • 反意义重叠增加了ORF出现的可能性.
  • 反意义重叠降低了ORF损失的可能性.
  • 这些效应在三种阅读框架之一中特别明显.

结论:

  • 这些发现合理化了在反意义转录中观察到的新基因的流行率.
  • 提供一种通用建模和分析框架,用于理解反意义的基因进化.