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Noncoding Centromeric RNA Expression Impairs Chromosome Stability in Human and Murine Stem Cells
- Source :
- Disease Markers, Disease Markers, Vol 2017 (2017)
- Publication Year :
- 2017
- Publisher :
- Hindawi, 2017.
-
Abstract
- We analyzed the effect of transcribed noncoding RNA centromeric satellites on chromosome segregation in normal human and murine stem and fibrosarcoma cells. The overexpression of different centromeric alphoid DNAs in all cell lines induced a marked increase in chromosome mis-segregation in anaphase. Overexpression of centromeric mouse minor satellite also increased chromosome instability in the murine stem but not in human cells. Analysis of chromosome segregation in vivo showed disturbances in the mitotic progression, which was frequently unresolved. Live cell imaging revealed that overexpression of centromeric satellites resulted in several different chromosomal morphological errors in the cell nuclei. Our findings correlated with other reports that several centromeric noncoding RNAs are detected in different carcinoma cells and their expression resulted in segregation errors. Our study furnishes further insights into a novel source of genomic instability in human and murine cells. It has recently been shown that noncoding centromeric RNAs are present in some form of cancer, and thus, overexpression of several types of centromeric noncoding RNAs may be useful as a specific maker for neoplastic cells.
- Subjects :
- 0301 basic medicine
Genome instability
RNA, Untranslated
Article Subject
Clinical Biochemistry
Centromere
Biology
Cell Line
Chromosome segregation
03 medical and health sciences
Mice
Chromosome instability
Cell Line, Tumor
Chromosomal Instability
Chromosome Segregation
Genetics
Animals
Humans
Molecular Biology
Anaphase
lcsh:R5-920
Stem Cells
Biochemistry (medical)
RNA
Chromosome
General Medicine
Non-coding RNA
Molecular biology
3. Good health
030104 developmental biology
Stem cell
lcsh:Medicine (General)
Research Article
Subjects
Details
- Language :
- English
- ISSN :
- 18758630 and 02780240
- Volume :
- 2017
- Database :
- OpenAIRE
- Journal :
- Disease Markers
- Accession number :
- edsair.doi.dedup.....4f71505195837ebaa1dae0b102926916