Drosophila ADCK1 is critical for maintaining mitochondrial structures and functions in the muscle.
The function of AarF domain-containing kinase 1 (ADCK1) has not been thoroughly revealed. Here we identified that ADCK1 utilizes YME1-like 1 ATPase (YME1L1) to control optic atrophy 1 (OPA1) and inner membrane mitochondrial protein (IMMT) in regulating mitochondrial dynamics and cristae structure. W...
| Main Authors: | , , , |
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| Format: | Article |
| Language: | English |
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Public Library of Science (PLoS)
2019-05-01
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| Series: | PLoS Genetics |
| Online Access: | https://doi.org/10.1371/journal.pgen.1008184 |
| _version_ | 1797350863428124672 |
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| author | Woongchang Yoon Sun-Hong Hwang Sang-Hee Lee Jongkyeong Chung |
| author_facet | Woongchang Yoon Sun-Hong Hwang Sang-Hee Lee Jongkyeong Chung |
| author_sort | Woongchang Yoon |
| collection | DOAJ |
| description | The function of AarF domain-containing kinase 1 (ADCK1) has not been thoroughly revealed. Here we identified that ADCK1 utilizes YME1-like 1 ATPase (YME1L1) to control optic atrophy 1 (OPA1) and inner membrane mitochondrial protein (IMMT) in regulating mitochondrial dynamics and cristae structure. We firstly observed that a serious developmental impairment occurred in Drosophila ADCK1 (dADCK1) deletion mutant, resulting in premature death before adulthood. By using temperature sensitive ubiquitously expression driver tub-Gal80ts/tub-Gal4 or muscle-specific expression driver mhc-Gal4, we observed severely defective locomotive activities and structural abnormality in the muscle along with increased mitochondrial fusion in the dADCK1 knockdown flies. Moreover, decreased mitochondrial membrane potential, ATP production and survival rate along with increased ROS and apoptosis in the flies further demonstrated that the structural abnormalities of mitochondria induced by dADCK1 knockdown led to their functional abnormalities. Consistent with the ADCK1 loss-of-function data in Drosophila, ADCK1 over-expression induced mitochondrial fission and clustering in addition to destruction of the cristae structure in Drosophila and mammalian cells. Interestingly, knockdown of YME1L1 rescued the phenotypes of ADCK1 over-expression. Furthermore, genetic epistasis from fly genetics and mammalian cell biology experiments led us to discover the interactions among IMMT, OPA1 and ADCK1. Collectively, these results established a mitochondrial signaling pathway composed of ADCK1, YME1L1, OPA1 and IMMT, which has essential roles in maintaining mitochondrial morphologies and functions in the muscle. |
| first_indexed | 2024-03-08T12:51:14Z |
| format | Article |
| id | doaj.art-38cb7c9c288e4c22907b64369f8758de |
| institution | Directory Open Access Journal |
| issn | 1553-7390 1553-7404 |
| language | English |
| last_indexed | 2024-03-08T12:51:14Z |
| publishDate | 2019-05-01 |
| publisher | Public Library of Science (PLoS) |
| record_format | Article |
| series | PLoS Genetics |
| spelling | doaj.art-38cb7c9c288e4c22907b64369f8758de2024-01-20T05:33:21ZengPublic Library of Science (PLoS)PLoS Genetics1553-73901553-74042019-05-01155e100818410.1371/journal.pgen.1008184Drosophila ADCK1 is critical for maintaining mitochondrial structures and functions in the muscle.Woongchang YoonSun-Hong HwangSang-Hee LeeJongkyeong ChungThe function of AarF domain-containing kinase 1 (ADCK1) has not been thoroughly revealed. Here we identified that ADCK1 utilizes YME1-like 1 ATPase (YME1L1) to control optic atrophy 1 (OPA1) and inner membrane mitochondrial protein (IMMT) in regulating mitochondrial dynamics and cristae structure. We firstly observed that a serious developmental impairment occurred in Drosophila ADCK1 (dADCK1) deletion mutant, resulting in premature death before adulthood. By using temperature sensitive ubiquitously expression driver tub-Gal80ts/tub-Gal4 or muscle-specific expression driver mhc-Gal4, we observed severely defective locomotive activities and structural abnormality in the muscle along with increased mitochondrial fusion in the dADCK1 knockdown flies. Moreover, decreased mitochondrial membrane potential, ATP production and survival rate along with increased ROS and apoptosis in the flies further demonstrated that the structural abnormalities of mitochondria induced by dADCK1 knockdown led to their functional abnormalities. Consistent with the ADCK1 loss-of-function data in Drosophila, ADCK1 over-expression induced mitochondrial fission and clustering in addition to destruction of the cristae structure in Drosophila and mammalian cells. Interestingly, knockdown of YME1L1 rescued the phenotypes of ADCK1 over-expression. Furthermore, genetic epistasis from fly genetics and mammalian cell biology experiments led us to discover the interactions among IMMT, OPA1 and ADCK1. Collectively, these results established a mitochondrial signaling pathway composed of ADCK1, YME1L1, OPA1 and IMMT, which has essential roles in maintaining mitochondrial morphologies and functions in the muscle.https://doi.org/10.1371/journal.pgen.1008184 |
| spellingShingle | Woongchang Yoon Sun-Hong Hwang Sang-Hee Lee Jongkyeong Chung Drosophila ADCK1 is critical for maintaining mitochondrial structures and functions in the muscle. PLoS Genetics |
| title | Drosophila ADCK1 is critical for maintaining mitochondrial structures and functions in the muscle. |
| title_full | Drosophila ADCK1 is critical for maintaining mitochondrial structures and functions in the muscle. |
| title_fullStr | Drosophila ADCK1 is critical for maintaining mitochondrial structures and functions in the muscle. |
| title_full_unstemmed | Drosophila ADCK1 is critical for maintaining mitochondrial structures and functions in the muscle. |
| title_short | Drosophila ADCK1 is critical for maintaining mitochondrial structures and functions in the muscle. |
| title_sort | drosophila adck1 is critical for maintaining mitochondrial structures and functions in the muscle |
| url | https://doi.org/10.1371/journal.pgen.1008184 |
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