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XB-ART-55255
Sci Rep January 1, 2018; 8 (1): 13035.

Ras-dva small GTPases lost during evolution of amniotes regulate regeneration in anamniotes.

Ivanova AS , Korotkova DD , Ermakova GV , Martynova NY , Zaraisky AG , Tereshina MB .


Abstract
In contrast to amniotes (reptiles, birds and mammals), anamniotes (fishes and amphibians) can effectively regenerate body appendages such as fins, limbs and tails. Why such a useful capability was progressively lost in amniotes remains unknown. As we have hypothesized recently, one of the reasons for this could be loss of some genes regulating the regeneration in evolution of amniotes. Here, we demonstrate the validity of this hypothesis by showing that genes of small GTPases Ras-dva1 and Ras-dva2, that had been lost in a stepwise manner during evolution of amniotes and disappeared completely in placental mammals, are important for regeneration in anamniotes. Both Ras-dva genes are quickly activated in regenerative wound epithelium and blastema forming in the amputated adult Danio rerio fins and Xenopus laevis tadpoles'' tails and hindlimb buds. Down-regulation of any of two Ras-dva genes in fish and frog resulted in a retardation of regeneration accompanied by down-regulation of the regeneration marker genes. On the other hand, Ras-dva over-expression in tadpoles'' tails restores regeneration capacity during the refractory period when regeneration is blocked due to natural reasons. Thus our data on Ras-dva genes, which were eliminated in amniotes but play role in anamniotes regeneration regulation, satisfy our hypothesis.

PubMed ID: 30158598
Article link: Sci Rep

Genes referenced: ag1 agr2 diras1 diras2 fgf20 fgf8 igf2bp3 msx1 nras psmd6 rab1a ran ras-dva1 ras-dva2 rasl10b rho rhoa
GO keywords: animal organ regeneration
Morpholinos: agr2 MO1 ras-dva1 MO1 ras-dva2 MO1


Article Images: [+] show captions
References:
Bachy, 2003, Pubmed, Xenbase [+]


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