Identification of Diverse Adenosine-to-Inosine RNA Editing Subtypes in Colorectal Cancer

Si-Hyun Lee1, Hwang-Phill Kim1,2, Jun-Kyu Kang1,2

  • 1Department of Molecular Medicine and Biopharmaceutical Sciences, Graduate School of Convergence Science and Technology, Seoul National University College of Medicine, Seoul, Korea.

Abstract

Insights

This study identified novel RNA editing patterns in colorectal cancer (CRC), revealing potential biomarkers for patient identification. Specific gene editing alterations were observed, distinguishing cancer from normal tissues.

Area of Science:

  • Molecular Biology
  • Genomics
  • Cancer Research

Background:

  • RNA editing diversifies proteins without altering DNA.
  • Adenosine-to-inosine (A-to-I) RNA editing is rare in colorectal cancer (CRC).

Purpose of the Study:

  • To identify diverse RNA editing patterns in human colorectal cancer (CRC).
  • To investigate nonsynonymous RNA editing in CRC.
  • To explore RNA editing as potential CRC biomarkers.

Main Methods:

  • Compared transcriptome data from 39 CRC samples and adjacent tissues.
  • Focused on canonical A-to-I RNA edits in coding regions.
  • Analyzed nonsynonymous RNA editing patterns.

Main Results:

  • Identified 10 recurrent nonsynonymous RNA editing candidates in nine genes.
  • Observed both hypo- and hyper-RNA editing patterns in CRC samples.
  • Found increased editing of GLI1 in cancer tissues, while most other genes were hypoedited.

Conclusions:

  • Nonsynonymous RNA editing patterns can distinguish CRC patients.
  • Identified RNA editing events may serve as novel biomarkers for CRC detection.

Related Concept Videos

RNA Editing02:23

RNA Editing

RNA editing is a post-transcriptional modification where a precursor mRNA (pre-mRNA) nucleotide sequence is changed by base insertion, deletion, or modification. The extent of RNA editing varies from a few hundred bases, in mitochondrial DNA of trypanosomes, to a just single base, in nuclear genes of mammals. Even a single base change in the pre-mRNA can convert a codon for one amino acid into the codon for another amino acid or a stop codon. This type of re-coding can significantly affect the...
10.0K
Experimental RNAi02:15

Experimental RNAi

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...
8.1K
Alternative RNA Splicing02:18

Alternative RNA Splicing

Alternative RNA splicing is the regulated splicing of exons and introns to produce different mature mRNAs from a single pre-mRNA. Unlike in constitutive splicing where a single gene produces a single type of mRNA, alternative splicing allows an organism to produce multiple proteins from a single gene and plays an important role in protein diversity.
There are five types of alternative RNA splicing that vary in the ways the pre-mRNA segments are removed or retained in the mature mRNA. The first...
25.5K
RNA Splicing01:32

RNA Splicing

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...
61.0K
Non-LTR Retrotransposons03:18

Non-LTR Retrotransposons

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...
13.7K
Pharmacogenetics of Drug Targets: β₂-Adrenergic Receptors, Apo E, Thymidylate Synthase01:11

Pharmacogenetics of Drug Targets: β₂-Adrenergic Receptors, Apo E, Thymidylate Synthase

Genetic polymorphisms in drug targets have emerged as critical determinants of interindividual variability in drug response and toxicity. Pharmacogenomic investigations increasingly focus on identifying these variations to personalize and optimize therapeutic interventions. A drug target may be a receptor, enzyme, or signaling protein involved in pharmacologic responses or disease-related pathways. While early pharmacogenetic studies focused primarily on drug metabolism, current research...
60