ID | 114930 |
Title Alternative | Insect Adenine Nucleotide Translocases
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Author |
Sugahara, Ryohei
National Institute of Agrobiological Sciences
Jouraku, Akiya
National Institute of Agrobiological Sciences
Nakakura, Takayo
National Institute of Agrobiological Sciences
Kusakabe, Takahiro
Kyushu University
Shinohara, Yasuo
University of Tokushima
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Miyoshi, Hideto
Kyoto University
Shiotsuki, Takahiro
National Institute of Agrobiological Sciences
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Content Type |
Journal Article
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Description | Mitochondrial adenine nucleotide translocase (ANT) specifically acts in ADP/ATP exchange through the mitochondrial inner membrane. This transporter protein thereby plays a significant role in energy metabolism in eukaryotic cells. Most mammals have four paralogous ANT genes (ANT1-4) and utilize these paralogues in different types of cells. The fourth paralogue of ANT (ANT4) is present only in mammals and reptiles and is exclusively expressed in testicular germ cells where it is required for meiotic progression in the spermatocytes. Here, we report that silkworms harbor two ANT paralogues, the homeostatic paralogue (BmANTI1) and the testis-specific paralogue (BmANTI2). The BmANTI2 protein has an N-terminal extension in which the positions of lysine residues in the amino acid sequence are distributed as in human ANT4. An expression analysis showed that BmANTI2 transcripts were restricted to the testis, suggesting the protein has a role in the progression of spermatogenesis. By contrast, BmANTI1 was expressed in all tissues tested, suggesting it has an important role in homeostasis. We also observed that cultured silkworm cells required BmANTI1 for proliferation. The ANTI1 protein of the lepidopteran Plutella xylostella (PxANTI1), but not those of other insect species (or PxANTI2), restored cell proliferation in BmANTI1-knockdown cells suggesting that ANTI1 has similar energy metabolism functions across the Lepidoptera. Our results suggest that BmANTI2 is evolutionarily divergent from BmANTI1 and has developed a specific role in spermatogenesis similar to that of mammalian ANT4.
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Journal Title |
PLOS ONE
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ISSN | 19326203
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Publisher | PLOS
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Volume | 10
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Issue | 3
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Start Page | e0119429
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Published Date | 2015-03-05
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Rights | © 2015 Sugahara et al. This is an open access article distributed under the terms of the Creative Commons Attribution License(https://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
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language |
eng
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departments |
Institute of Advanced Medical Sciences
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