Cloning, ontogenesis, and localization of an atypical uncoupling protein 4 inXenopus laevis

Author:

Keller Patrick A.1,Lehr Lorenz1,Giacobino Jean-Paul1,Charnay Yves2,Assimacopoulos-Jeannet Françoise1,Giovannini Natalia1

Affiliation:

1. Department of Cell Physiology and Metabolism, University Medical Center 1, Geneva

2. Division of Neuropsychiatry, Belle-Idée, Geneva University Hospital, Chene-Bourg, Switzerland

Abstract

Uncoupling protein 1 (UCP1) is the first UCP described. It belongs to the family of mitochondrial carrier proteins and is expressed mainly in brown adipose tissue. Recently, the family of the UCPs has rapidly been growing due to the successive cloning of UCP2, UCP3, UCP4, and UCP5, also called brain mitochondrial carrier protein 1. Phylogenetic studies suggest that UCP1/UCP2/UCP3 on one hand and UCP4/UCP5 on the other hand belong to separate subfamilies. In this study, we report the cloning from a frog Xenopus laevis (Xl) oocyte cDNA library of a novel UCP that was shown, by sequence homology, to belong to the family of ancestral UCP4. This cloning provides a milestone in the gap between Drosophila melanogaster or Caenorhabditis elegans on one hand and mammalian UCP4 on the other. Xl UCP4 is already expressed in the oocyte, being the first UCP described in germ cell lineage. During development, it segregates in the neural cord, and, in the adult, in situ hybridization shows its expression in the neurons and also in the choroid plexus of the brain. By RT-PCR analysis, it was found that Xl UCP4 is present in all the subdivisions of the brain and also that it differs from mammalian UCP4 by a very high relative level of expression in peripheral tissues such as the liver and kidney. The peripheral tissue distribution of Xl UCP4 reinforces the hypothesis that UCP4 might be the ancestral UCP from which other UCPs diverged from.

Publisher

American Physiological Society

Subject

Genetics,Physiology

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