Computational methods for direct cell conversion. Issue 24 (16th December 2016)
- Record Type:
- Journal Article
- Title:
- Computational methods for direct cell conversion. Issue 24 (16th December 2016)
- Main Title:
- Computational methods for direct cell conversion
- Authors:
- Kamaraj, Uma S.
Gough, Julian
Polo, Jose M.
Petretto, Enrico
Rackham, Owen J. L. - Abstract:
- ABSTRACT: Directed cell conversion (or transdifferentiation) of one somatic cell-type to another can be achieved by ectopic expression of a set of transcription factors. Since the experimental identification of transcription factors for transdifferentiation is extremely time-consuming and expensive, there are still relatively few transdifferentiations achieved in comparison to the number of human cell-types. However, the growing volume of transcriptional data available and the recent introduction of data-driven algorithmic approaches that predict factors for transdifferentiation holds great promise for accelerating this field. Here we review those computational methods whose in-silico predictions have been experimentally validated, highlighting differences and similarities. Our analysis reveals that the factors predicted by each method tend to be different due to varying source cells used, gene expression quantification and algorithmic steps. We show these differences have an impact on the regulatory influences downstream, with some methods favoring transcription factors regulating developmental progression and others favoring factors regulating mature cell processes. These computational approaches offer a starting point to predict and test novel factors for transdifferentiation. We argue that collecting high-quality gene expression data from single-cells or pure cell-populations across a broader set of cell-types would be necessary to improve the quality and consistency ofABSTRACT: Directed cell conversion (or transdifferentiation) of one somatic cell-type to another can be achieved by ectopic expression of a set of transcription factors. Since the experimental identification of transcription factors for transdifferentiation is extremely time-consuming and expensive, there are still relatively few transdifferentiations achieved in comparison to the number of human cell-types. However, the growing volume of transcriptional data available and the recent introduction of data-driven algorithmic approaches that predict factors for transdifferentiation holds great promise for accelerating this field. Here we review those computational methods whose in-silico predictions have been experimentally validated, highlighting differences and similarities. Our analysis reveals that the factors predicted by each method tend to be different due to varying source cells used, gene expression quantification and algorithmic steps. We show these differences have an impact on the regulatory influences downstream, with some methods favoring transcription factors regulating developmental progression and others favoring factors regulating mature cell processes. These computational approaches offer a starting point to predict and test novel factors for transdifferentiation. We argue that collecting high-quality gene expression data from single-cells or pure cell-populations across a broader set of cell-types would be necessary to improve the quality and consistency of the in-silico predictions. … (more)
- Is Part Of:
- Cell cycle. Volume 15:Issue 24(2016)
- Journal:
- Cell cycle
- Issue:
- Volume 15:Issue 24(2016)
- Issue Display:
- Volume 15, Issue 24 (2016)
- Year:
- 2016
- Volume:
- 15
- Issue:
- 24
- Issue Sort Value:
- 2016-0015-0024-0000
- Page Start:
- 3343
- Page End:
- 3354
- Publication Date:
- 2016-12-16
- Subjects:
- algorithm -- prediction -- transcription factor -- transdifferentiation
Cell cycle -- Periodicals
571.84377 - Journal URLs:
- http://www.tandfonline.com/ ↗
http://www.tandfonline.com/toc/kccy20/current ↗ - DOI:
- 10.1080/15384101.2016.1238119 ↗
- Languages:
- English
- ISSNs:
- 1538-4101
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3097.746500
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 255.xml