bioRxiv Science⌕ Search

Biology subjects

Carnicero, P.

Publications and source records attributed to Carnicero, P..

2 recordsLinked to original sources

Spatiotemporal diversification of forest understorey species reveals the existence of multiple Pleistocene forest refugia in Central Europe

During Pleistocene cold stages, European temperate forests were not only restricted to refugia in the southern European peninsulas. Rather, there is increasing evidence for survival of trees also in isolated patches further north, termed "northern refugia". While their existence is undisputed, based on what is known from a handful of tree species, there is very limited knowledge about forest understoreys. Here, we fill this gap by examining the evolutionary histories of three Central European forest understorey species (FUS; Aposeris foetida, Cardamine trifolia, Hacquetia epipactis). To do so, we use a set of exploratory and explicit analyses utilizing genomic data and ecological niche models, and interpret these data following an a priori defined framework. We identify the northwestern Balkan Peninsula as the primary diversification center for the three species but found additional northern refugia in the Alps, the Carpathians, and the Apennines. Divergence times indicated pre-Last Glacial Maximum (LGM) diversification within each FUS, suggesting persistence of forest islands in Central Europe during Pleistocene cold stages rather than exclusively post-LGM colonization. We conclude that FUS thrived in scattered northern refugia. This refines our understanding of past forest dynamics and further supports widespread long-term persistence of forest patches in Central Europe during Pleistocene cold stages.

evolutionary biology↗

Proteostasis control via HSP90α sustains YAP activity to drive aggressive behaviours in cancer-associated fibroblasts

Cancers adapt proteostasis to cope with the burden of misfolded proteins, stabilize key signalling nodes and sustain their malignant behaviour. Tumour stroma is subjected to similar stresses, but how they influence its aberrant status remains unclear. We show that tumour stroma presents consistent upregulation of target genes associated to the major misfolding regulator HSP90 in cancer-associated fibroblasts (CAFs), and that HSP90 is required for CAFs to remodel the extracellular matrix (ECM) and promote cancer cell motility and growth. Mechanistically, HSP90 sustains TGF{beta} responses and YAP protein levels required for CAF functionality. In vivo, stromal or fibroblast-specific loss of HSP90 results in reduced ECM deposition, angiogenesis, growth and dissemination of breast tumours. Clinical analyses reveal a correlation between HSP90-dependent programs and YAP activity in CAFs, that are also associated with poor patient prognosis. Our findings uncover a link between proteostasis, mechanotransduction and generation of aggressive tumour microenvironments through HSP90.

cancer biology↗