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Dahan, T.

Publications and source records attributed to Dahan, T..

2 recordsLinked to original sources

Evidence for a reproductive sharing continuum in cooperatively breeding mammals and birds: consequences for comparative research

Extreme reproductive skew occurs when a dominant female/male monopolises reproduction within a group of multiple sexually mature females/males. It is sometimes considered an additional, restrictive criterion in the definition of cooperative breeding (i.e., when conspecifics provide parental care to other group members offspring). However, datasets that use this restrictive definition to classify species as cooperative breeders have two critical shortcomings. First, reproductive skew is systematically overestimated by including groups with a single sexually mature female/male when calculating the reproductive output of "dominant" females/males. Second, a lack of reporting on which species are classified based on limited data prevents accounting for uncertainty in classification. Considering these shortcomings, we show that extreme reproductive skew in multi-female and multi-male groups only occurs rarely in species previously classified as cooperative breeders using restrictive definitions (11 mammal species, 12 bird species). We further provide updated datasets on reproductive sharing in multi-female/male groups of cooperatively breeding mammals and birds that allow accounting for classification uncertainty. Our results demonstrate a reproductive sharing continuum even among those cooperatively breeding species argued to exhibit extreme reproductive skew. At the practical level, these findings call for significant changes in datasets that classify species by social systems. At the conceptual level, we suggest that reproductive skew should not be a defining criterion of cooperative breeding.

animal behavior and cognition↗

Species-specific roles for the MAFA and MAFB transcription factors in regulatingislet β cell identity

Type 2 diabetes (T2D) is associated with compromised identity of insulin-producing pancreatic islet beta ({beta}) cells, characterized by inappropriate production of other islet cell-enriched hormones. Here we examined how hormone misexpression was influenced by the MAFA and MAFB transcription factors, closely related proteins that maintain islet cell function. Mice specifically lacking MafA in {beta} cells demonstrated broad, population-wide changes in hormone gene expression with an overall gene signature closely resembling islet gastrin (Gast)-positive cells generated under conditions of chronic hyperglycemia and obesity. A human {beta} cell line deficient in MAFB, but not one lacking MAFA, also produced a gastrin (GAST)-positive gene expression pattern. In addition, GAST was detected in human T2D {beta} cells with low levels of MAFB. Moreover, evidence is provided that human MAFB can directly repress GAST gene transcription. These results support a novel, species-specific role for MafA and MAFB in maintaining adult mouse and human {beta} cell identity, respectively, by repressing expression of Gast/GAST and other non-{beta} cell hormones.

cell biology↗