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Related Concept Videos

piRNA - Piwi-interacting RNAs02:57

piRNA - Piwi-interacting RNAs

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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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DNA-only Transposons02:57

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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...
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Overview of Transposition and Recombination02:13

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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...
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RNA Interference01:23

RNA Interference

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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.
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...
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Non-LTR Retrotransposons03:18

Non-LTR Retrotransposons

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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...
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A Computational Pipeline for Intergenic/Intragenic Enhancer RNA Quantification in Mouse Embryonic Stem Cells
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A genetic algorithm-based weighted ensemble method for predicting transposon-derived piRNAs.

Dingfang Li1, Longqiang Luo1, Wen Zhang2,3

  • 1School of Mathematics and Statistics, Wuhan University, Wuhan, 430072, China.

BMC Bioinformatics
|September 1, 2016
PubMed
Summary
This summary is machine-generated.

A new genetic algorithm-based method accurately predicts transposon-derived piwi-interacting RNAs (piRNAs) in humans, mice, and Drosophila. This approach shows promise for advancing gamete generation research.

Keywords:
Ensemble learningFeatureGenetic algorithmpiRNA

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Area of Science:

  • Bioinformatics
  • Genomics
  • Molecular Biology

Background:

  • piwi-interacting RNA (piRNA) prediction is crucial for understanding gamete generation.
  • Existing machine learning methods for piRNA prediction require further improvement.

Purpose of the Study:

  • To develop an improved method for predicting transposon-derived piRNAs.
  • To evaluate the proposed method's performance across different species and dataset types.

Main Methods:

  • A genetic algorithm-based weighted ensemble method was developed.
  • Prediction models were constructed and evaluated using balanced and imbalanced datasets for Human, Mouse, and Drosophila.
  • Cross-species prediction capabilities were assessed.

Main Results:

  • The proposed method achieved high AUC values (0.932-0.996) on both balanced and imbalanced datasets across species.
  • The models demonstrated strong performance in cross-species piRNA identification.
  • The method outperformed existing state-of-the-art approaches.

Conclusions:

  • The genetic algorithm-based weighted ensemble method offers a promising approach for transposon-derived piRNA prediction.
  • The developed models exhibit robust performance and potential for broader applications in piRNA research.
  • Source code and datasets are publicly available for reproducibility.