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Related Concept Videos

Nuclear Localization Signals and Import01:46

Nuclear Localization Signals and Import

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Proteins targeted to the nucleus carry short stretches of amino acid sequences called the nuclear localization signal or NLS. Classical nuclear localization signals are of two types: monopartite and bipartite NLS. Monopartite classical NLS (cNLS) consists of a single cluster of 4-8 amino acids. Bipartite cNLS consists of two clusters of  2-3 amino acids and a 9-12 residue long proline-rich linker bridging the two clusters. Signal clusters are rich in positively charged amino acids such as...
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The nucleolus is the most prominent substructure of the nucleus. When it was first discovered, it was considered to be an isolated organelle that forms fibrils and granules. In 1931, the relationship between the nucleolus and chromosomes was first described by Heitz. He observed that the appearance and size of nucleolus varies depending on the stage of the cell cycle. He also noticed constricted regions on different chromosomes clustered together at definite cell cycle stages. These regions,...
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Ribosome profiling or ribo-sequencing is a deep sequencing technique that produces a snapshot of active translation in a cell. It selectively sequences the mRNAs protected by ribosomes to get an insight into a cell’s translation landscape at any given point in time.
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The pentose sugar in DNA is deoxyribose, while in RNA the pentose sugar is ribose. The difference between the sugars is the presence of the hydroxyl group on the ribose's second carbon and a hydrogen on the deoxyribose's second carbon. The phosphate residue attaches to the hydroxyl group of the 5′ carbon of one sugar and the hydroxyl group of the 3′ carbon of the sugar of the next nucleotide, which forms  a 5′ to 3′ phosphodiester linkage.
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RNA sequencing, or RNA-Seq, is a high-throughput sequencing technology used to study the transcriptome of a cell. Transcriptomics helps to interpret the functional elements of a genome and identify the molecular constituents of an organism. Additionally, it also helps in understanding the development of an organism and the occurrence of diseases. 
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During most eukaryotic translation processes, the small 40S ribosome subunit scans an mRNA from its 5' end until it encounters the first start AUG codon. The large 60S ribosomal subunit then joins the smaller one to initiate protein synthesis. The location of the translation initiation is largely determined by the nucleotides near the start codon as there may be multiple translation initiation sites present on the mRNA.  Marilyn Kozak discovered that the sequence RCCAUGG (where R...
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RNAlight: a machine learning model to identify nucleotide features determining RNA subcellular localization.

Guo-Hua Yuan1, Ying Wang1, Guang-Zhong Wang1

  • 1CAS Key Laboratory of Computational Biology, Shanghai Institute of Nutrition and Health, University of Chinese Academy of Sciences, Chinese Academy of Sciences, Shanghai 200031, China.

Briefings in Bioinformatics
|December 4, 2022
PubMed
Summary
This summary is machine-generated.

This study introduces RNAlight, a machine learning model that identifies nucleotide sequences determining RNA subcellular localization. The model accurately predicts localization for various RNA types, revealing sequence-based mechanisms.

Keywords:
RNA binding proteinRNA localizationcircular RNAmachine learningmotifnucleotide feature

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Area of Science:

  • Molecular Biology
  • Bioinformatics
  • Computational Biology

Background:

  • RNAs exhibit diverse subcellular localizations, crucial for their function.
  • Nucleotide features dictating messenger RNA (mRNA) and long non-coding RNA (lncRNA) localization remain incompletely understood.

Purpose of the Study:

  • To develop a machine learning model, RNAlight, for identifying nucleotide features that determine mRNA and lncRNA subcellular localization.
  • To elucidate the sequence basis for distinct RNA distributions within the cell.

Main Methods:

  • Utilized LightGBM machine learning model to analyze nucleotide k-mers.
  • Employed the Tree SHAP algorithm to extract sequence features associated with cytoplasmic or nuclear localization.
  • Mapped identified k-mers to RNA-binding protein (RBP)-associated motifs.

Main Results:

  • Identified specific nucleotide k-mers contributing to mRNA and lncRNA subcellular localization.
  • Uncovered distinct sequence features and associated RBPs for RNAs localized in the cytoplasm versus the nucleus.
  • Demonstrated RNAlight's generalizability by accurately predicting subcellular localization for snRNAs, snoRNAs, and circular RNAs.

Conclusions:

  • RNAlight effectively identifies sequence determinants of RNA subcellular localization.
  • The findings highlight a sequence-based mechanism underlying distinct RNA distributions.
  • RNAlight offers a versatile tool for predicting subcellular localization across diverse RNA types.