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Jaime H. Reina

Researcher at University of Lausanne

Publications -  6
Citations -  676

Jaime H. Reina is an academic researcher from University of Lausanne. The author has contributed to research in topics: Transcriptional regulation & RNA polymerase II. The author has an hindex of 6, co-authored 6 publications receiving 598 citations.

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Defining the RNA polymerase III transcriptome: Genome-wide localization of the RNA polymerase III transcription machinery in human cells.

TL;DR: The results reveal broad usage of the known Pol III transcription machinery and define a minimal Pol III transcriptome in dividing IMR90hTert fibroblasts, which does not contain any of the microRNA genes previously described as transcribed by Pol III, but reveals two other micro RNA genes, MIR886 and MIR1975, which are genuine PolIII transcription units.
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mTORC1 Directly Phosphorylates and Regulates Human MAF1

TL;DR: The results describe molecular mechanisms by which mTORC1 controls human MAF1, a key repressor of RNA polymerase III transcription, and add a new branch to the signal transduction cascade immediately downstream of TORC1.
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Ligands for pheromone-sensing neurons are not conformationally activated odorant binding proteins.

TL;DR: An in vivo functional analysis of an odorant binding protein in Drosophila challenges the established model of its role in pheromone signaling.
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Maf1, a new player in the regulation of human RNA polymerase III transcription.

TL;DR: It is shown that human endogenous Maf1 can be co-immunoprecipitated with pol III and associates in vitro with two pol III subunits, the largest subunit RPC1 and the α-like subunit RPAC2, which suggest that Maf 1 is a major regulator of pol III transcription in human cells.
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A CD36 ectodomain mediates insect pheromone detection via a putative tunnelling mechanism

TL;DR: A model in which SNMP1 funnels hydrophobic pheromones from the extracellular fluid to integral membrane receptors is proposed, in which this ectodomain is essential, but intracellular and transmembrane domains dispensable, for cilia localization and phersomone-evoked responses.