Diversification of mineralocorticoid receptor genes in a subterranean rodent, the naked mole-rat

Author:

Oka Kaori1,Bono Hidemasa2,Kuroiwa Asato3,Fujioka Shusuke4,Shimizu Atsushi5,Katsu Yoshinao6,Miura Kyoko7

Affiliation:

1. K Oka, Department of Aging and Longevity Research, Faculty of Life Sciences, Kumamoto University, Kumamoto, Japan

2. H Bono, Program of Biomedical Science, Graduate School of Integrated Sciences for Life, Hiroshima University, Higashihiroshima, Japan

3. A Kuroiwa, Division of Reproductive and Developmental Biology, Department of Biological Sciences, Faculty of Science, Hokkaido University, Sapporo, Japan

4. S Fujioka, Department of Aging and Longevity Research, Faculty of Life Sciences, Kumamoto University, Kumamoto, Japan

5. A Shimizu, Division of Biomedical Information Analysis, Institute for Biomedical Sciences, Iwate Medical University, Morioka, Japan

6. Y Katsu, Division of Reproductive and Developmental Biology, Department of Biological Sciences, Faculty of Science, Hokkaido University, Sapporo, Japan

7. K Miura, Department of Aging and Longevity Research, Faculty of Life Sciences, Kumamoto University, Kumamoto, Japan

Abstract

Naked mole-rats (Heterocephalus glaber) inhabit subterranean burrows in savannas and are thus unable to access free water. To identify their mechanism of osmoregulation in xeric environments, we molecularly cloned and analyzed the mineralocorticoid receptor (MR) gene, required for hormone-dependent regulation of genes contributing to body fluid homeostasis. Most vertebrates harbor a single MR homolog. In contrast, we discovered that MR is duplicated in naked mole-rats. The amino acid sequence of naked mole-rat MR1 is 90% identical to its mouse ortholog, and MR1 is abundantly expressed in the kidney and the nervous system. MR2 encodes a truncated protein lacking DNA- and ligand-binding domains of MR1 and is expressed in diverse tissues. Although MR2 did not directly transactivate gene expression, it increased corticosteroid-dependent transcriptional activity of MR1. Our results suggest that MR2 might function as a novel regulator of MR1 activity to fine-tune MR signaling in naked mole-rats.

Publisher

Bioscientifica

Subject

Endocrinology,Molecular Biology

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