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Tarikere, S.

Publications and source records attributed to Tarikere, S..

2 recordsLinked to original sources

Chinmo is a novel regulator of differential Hippo signaling response within a single developing organ.

Orchestrated control of proliferation of multiple cell types is essential for building a healthy organ. Here we use larval ovary development in Drosophila melanogaster as a model to understand the homeostasis of somatic and germ line cells in the formation of the female adult reproductive organ. We previously showed that the highly conserved Hippo signaling pathway regulates proliferation of both germ line and somatic cells in the D. melanogaster larval ovary. Response to Hippo signaling appeared to be mediated by different genetic mechanisms in germ line and soma, but the mechanism allowing distinct responses to the same signaling pathway remained unknown. Here we perform cell type-specific RNA-Seq of isolated germ line and somatic cells from the developing ovary at multiple time points spanning the formation of germ line stem cell niches, in either a Hippo signaling loss- or gain-of-function genetic background. Applying network analysis to these data revealed a novel regulator of ovarian development, the transcription factor chinmo. Subsequent experimental validation showed that chinmo acts as a key germ cell-specific translator of Hippo signaling in the developing ovary, allowing the Hippo signal to be transduced in cell type-specific ways in germ line and somatic cells within the same organ.

developmental biology↗

Diverse genetic architectures on the Z chromosome underlie the two rules of speciation in Papilio butterfly hybrids

The fitness of animal hybrids follows two empirical rules: hybrids of the heterogametic sex aremore unfit (Haldanes Rule), and the sex chromosome is disproportionately involved in incompatibility (the large-X/Z effect). Whether these rules result from genetic mechanisms shared across taxa remains unknown, and existing explanations rarely consider female heterogametic taxa such as butterflies. Here, we investigate hybrid incompatibilities in Papilio and Heliconius butterflies, and show that defects coincide with unbalanced introgression between the Z chromosome and its genetic background. This polygenic mechanism predicts both rules because introgressed ancestry on the Z chromosome is more skewed in females, and is more variable than on all autosomes. Therefore, the explanation for both rules in butterflies shares little similarity with prevailing theories relying on dominance.

evolutionary biology↗