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Mironov, S.

Publications and source records attributed to Mironov, S..

2 recordsLinked to original sources

Tripartite networks show that keystone species can multitask

Keystone species are disproportionately important for ecosystem functioning (1,2). However, while all species engage in multiple interaction types with other species, the importance of keystone species is often defined based on a single dimension of their Eltonian niche (3), that is, one type of interaction (e.g., keystone predator). Therefore, it remains unclear whether the importance of keystone species is unidimensional or if it extends across interaction types. We conducted a meta-analysis of tripartite interaction networks to examine whether species importance in one dimension of their niche is mirrored in other niche dimensions, and whether this is associated with interaction outcome, intimacy, or species richness. We show that keystone species importance is positively associated across multiple ecological niche dimensions, independently of species abundance, and find no evidence that multidimensionality of keystone species is influenced by the explanatory variables. We propose that the role of keystone species extends across multiple ecological niche dimensions, with important implications for ecosystem resilience and conservation. Significance StatementKeystone species are often identified by focusing on a single type of interaction (e.g., predation, pollination, herbivory) which contrasts with the multiple roles that species play in biological communities. We conducted a meta-analysis of 18 tripartite interaction networks to explore if keystonness is correlated across the multiple dimensions of species Eltonian niches. Our results suggest that species importance tends to span across multiple interaction types, independently from abundance, which can be key to understand community resilience and collapse in face of multiple threats.

ecology

An EMT-primary cilium-GLIS2 signaling axis regulates mammogenesis and claudin-low breast tumorigenesis

The Epithelial-Mesenchymal Transition (EMT) and primary ciliogenesis induce stem cell properties in basal Mammary Stem Cells (MaSCs) to promote mammogenesis, but the underlying mechanisms remain incompletely understood. Here, we show that EMT transcription factors promote ciliogenesis at intermediate EMT transition states by activating ciliogenesis inducers, including FGFR1. The resulting primary cilia promote BBS11-dependent ubiquitination and inactivation of a central signaling node, GLIS2. We show that GLIS2 inactivation promotes MaSC stemness, and GLIS2 is required for normal mammary gland development. Moreover, GLIS2 inactivation is required to induce the proliferative and tumorigenic capacities of the Mammary-Tumor-initiating cells (MaTICs) of claudin-low breast cancers. Claudin-low breast tumors can be segregated from other breast tumor subtypes based on a GLIS2-dependent gene expression signature. Collectively, our findings establish molecular mechanisms by which EMT programs induce ciliogenesis to control MaSC and MaTIC biology, mammary gland development, and claudin-low breast cancer formation.

cell biology