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Transcriptome profiling reveals distinctive traits of retinol metabolism and neonatal parallels in the MRL/MpJ mouse

Authors :
Justyna Podolak-Popinigis
Anna Ronowicz
Paweł Sachadyn
Bartosz Górnikiewicz
Source :
BMC Genomics
Publisher :
Springer Nature

Abstract

Background The MRL/MpJ mouse is a laboratory inbred strain known for regenerative abilities which are manifested by scarless closure of ear pinna punch holes. Enhanced healing responses have been reported in other organs. A remarkable feature of the strain is that the adult MRL/MpJ mouse retains several embryonic biochemical characteristics, including increased expression of stem cell markers. Results We explored the transcriptome of the MRL/MpJ mouse in the heart, liver, spleen, bone marrow and ears. We used two reference strains, thus increasing the chances to discover the genes responsible for the exceptional properties of the regenerative strain. We revealed several distinctive characteristics of gene expression patterns in the MRL/MpJ mouse, including the repression of immune response genes, the up-regulation of those associated with retinol metabolism and PPAR signalling, as well as differences in expression of the genes engaged in wounding response. Another crucial finding is that the gene expression patterns in the adult MRL/MpJ mouse and murine neonates share a number of parallels, which are also related to immune and wounding response, PPAR pathway, and retinol metabolism. Conclusions Our results indicate the significance of retinol signalling and neonatal transcriptomic relics as the distinguishing features of the MRL/MpJ mouse. The possibility that retinoids could act as key regulatory molecules in this regeneration model brings important implications for regenerative medicine. Electronic supplementary material The online version of this article (doi:10.1186/s12864-015-2075-2) contains supplementary material, which is available to authorized users.

Details

Language :
English
ISSN :
14712164
Volume :
16
Issue :
1
Database :
OpenAIRE
Journal :
BMC Genomics
Accession number :
edsair.doi.dedup.....64d37b850601f6f581a71d6097f55d18
Full Text :
https://doi.org/10.1186/s12864-015-2075-2