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Isolation of Adult Spinal Cord Nuclei for Massively Parallel Single-nucleus RNA Sequencing
Published on: October 12, 2018
Comparative analysis of human protein-coding and noncoding RNAs between brain and 10 mixed cell lines by RNA-Seq
Geng Chen1, Kangping Yin, Leming Shi
1Center for Bioinformatics and Computational Biology, and the Institute of Biomedical Sciences, College of Life Science, East China Normal University, Shanghai, China.
Plos One
|December 6, 2011
Summary
Gene expression differences arise from varied isoforms, not just gene presence. This study highlights the importance of analyzing gene isoforms and long noncoding RNAs in understanding human cancers and the transcriptome.
Area of Science:
- Transcriptomics
- Genomics
- Molecular Biology
Background:
- Genes produce diverse functional products, including protein-coding and noncoding RNAs.
- Understanding gene expression complexity requires analyzing isoforms and noncoding RNAs.
Purpose of the Study:
- Investigate protein-coding capacities and isoform expression levels of human genes.
- Analyze conservation and disease association of long noncoding RNAs (ncRNAs).
Main Methods:
- Comparative analysis of transcriptome sequencing datasets from human brain and cell lines.
- Identification and characterization of long noncoding RNAs.
- RT-PCR validation of differentially expressed long ncRNAs.
Main Results:
- Significant differences in expressed isoforms between brain and cell lines, even for common genes.
- 282 human genes identified to produce both protein-coding and noncoding RNAs via alternative splicing.
- Over 1,000 long ncRNAs identified, many with conserved elements across species.
- Several long ncRNAs showed differential expression in breast and lung cancers, correlating with cancer-related genes.
Conclusions:
- Transcriptome differences are largely driven by isoform variation.
- Isoform-level analysis is crucial for a complete understanding of the transcriptome.
- Long ncRNAs play significant roles in human cancers and warrant further investigation.
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