Abstract
In vertebrates, the four transcription factors Sox2, c-Myc, Pou5f1 and Klf4 are involved in the differentiation of several tissues during vertebrate embryogenesis; moreover, they are normally co-expressed in embryonic stem cells and play roles in pluripotency, self-renewal, and maintenance of the undifferentiated state in adult cells. The in vitro forced co-expression of these factors, named Yamanaka factors (YFs), induces pluripotency in human or mouse fibroblasts. Botryllus schlosseri is a colonial tunicate undergoing continuous stem cell-mediated asexual development, providing a valuable model system for the study of pluripotency in the closest living relatives of vertebrates. In this study, we identified B. schlosseri orthologs of human Sox2 and c-Myc genes, as well as the closest homologs of the vertebrate-specific Pou5f1 gene, through an in-depth evolutionary analysis of the YF gene families in tunicates and other deuterostomes. Then, we studied the expression of these genes during the asexual cycle of B. schlosseri using in situ hybridization in order to investigate their possible involvement in tissue differentiation and in pluripotency maintenance. Our results show a shared spatio-temporal expression pattern consistent with the reported functions of these genes in invertebrate and vertebrate embryogenesis. Moreover, Myc, SoxB1 and Pou3 were expressed in candidate stem cells residing in their niches, while Pou2 was found expressed exclusively in the immature previtellogenic oocytes, both in gonads and circulating in the colonial vascular system. Our data suggest that Myc, SoxB1 and Pou3 may be individually involved in the differentiation of the same territories seen in other chordates, and that, together, they may play a role in stemness even in this colonial ascidian.
Highlights
Stem cells (SCs) are undifferentiated cells capable of selfrenewal and with the ability to differentiate into specialised cells
In this study we investigate the presence and the evolution of the Yamanaka factors (YFs) genes in ascidians, and analyze when and where the orthologs of the vertebrate YF genes are expressed in the blastogenetic cycle of B. schlosseri by using in situ hybridization (ISH) experiments
A single Myc gene was present in B. schlosseri and in all the other ascidians and invertebrate deuterostomes analyzed, and our evolutionary tree clearly shows that this single gene gave rise to the three vertebrate paralogs (L-Myc, N-Myc and C-Myc) through two duplication rounds (Figure 2A)
Summary
Stem cells (SCs) are undifferentiated cells capable of selfrenewal and with the ability to differentiate into specialised cells. Tunicates are the sister group of vertebrates (Delsuc et al, 2006), and colonial tunicates are the only chordates able to regenerate entire organisms from circulating SCs (Rinkevich et al, 1995; Sunanaga et al, 2006; Voskoboynik et al, 2007; Brown et al, 2009; Kassmer et al, 2019; Manni et al, 2019; Scelzo et al, 2019). As such, this group offers unique opportunities to investigate the similarities and differences in SC biology between vertebrate and invertebrate chordates. The ascidian Botryllus schlosseri is recognized as a model species for the study of SCs and asexual reproduction (Manni et al, 2007; Voskoboynik and Weissman, 2015; Manni et al, 2019) This species reproduces both sexually and asexually. Cell islands are numerous in adult individuals belonging to early-cycle colonies and decrease in number toward the latecycle. cSCs reside and proliferate in these transient niches and migrate before takeover through the haemocoel to relocate in newly formed niches of the following generations (Rinkevich et al, 2013)
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