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African Swine Fever Virus Protein E199L Promotes Cell Autophagy through the Interaction of PYCR2
African swine fever virus (ASFV), as a member of the large DNA viruses, may regulate autophagy and apoptosis by inhibiting programmed cell death. However, the function of ASFV proteins has not been fully elucidated, especially the role of autophagy in ASFV infection. One of three Pyrroline-5-carboxy...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Singapore
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8027715/ https://www.ncbi.nlm.nih.gov/pubmed/33830435 http://dx.doi.org/10.1007/s12250-021-00375-x |
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author | Chen, Sheng Zhang, Xinheng Nie, Yu Li, Hongxin Chen, Weiguo Lin, Wencheng Chen, Feng Xie, Qingmei |
author_facet | Chen, Sheng Zhang, Xinheng Nie, Yu Li, Hongxin Chen, Weiguo Lin, Wencheng Chen, Feng Xie, Qingmei |
author_sort | Chen, Sheng |
collection | PubMed |
description | African swine fever virus (ASFV), as a member of the large DNA viruses, may regulate autophagy and apoptosis by inhibiting programmed cell death. However, the function of ASFV proteins has not been fully elucidated, especially the role of autophagy in ASFV infection. One of three Pyrroline-5-carboxylate reductases (PYCR), is primarily involved in conversion of glutamate to proline. Previous studies have shown that depletion of PYCR2 was related to the induction of autophagy. In the present study, we found for the first time that ASFV E199L protein induced a complete autophagy process in Vero and HEK-293T cells. Through co-immunoprecipitation coupled with mass spectrometry (CoIP-MS) analysis, we firstly identified that E199L interact with PYCR2 in vitro. Importantly, our work provides evidence that E199L down-regulated the expression of PYCR2, resulting in autophagy activation. Overall, our results demonstrate that ASFV E199L protein induces complete autophagy through interaction with PYCR2 and down-regulate the expression level of PYCR2, which provide a valuable reference for the role of autophagy during ASFV infection and contribute to the functional clues of PYCR2. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s12250-021-00375-x. |
format | Online Article Text |
id | pubmed-8027715 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Springer Singapore |
record_format | MEDLINE/PubMed |
spelling | pubmed-80277152021-04-08 African Swine Fever Virus Protein E199L Promotes Cell Autophagy through the Interaction of PYCR2 Chen, Sheng Zhang, Xinheng Nie, Yu Li, Hongxin Chen, Weiguo Lin, Wencheng Chen, Feng Xie, Qingmei Virol Sin Research Article African swine fever virus (ASFV), as a member of the large DNA viruses, may regulate autophagy and apoptosis by inhibiting programmed cell death. However, the function of ASFV proteins has not been fully elucidated, especially the role of autophagy in ASFV infection. One of three Pyrroline-5-carboxylate reductases (PYCR), is primarily involved in conversion of glutamate to proline. Previous studies have shown that depletion of PYCR2 was related to the induction of autophagy. In the present study, we found for the first time that ASFV E199L protein induced a complete autophagy process in Vero and HEK-293T cells. Through co-immunoprecipitation coupled with mass spectrometry (CoIP-MS) analysis, we firstly identified that E199L interact with PYCR2 in vitro. Importantly, our work provides evidence that E199L down-regulated the expression of PYCR2, resulting in autophagy activation. Overall, our results demonstrate that ASFV E199L protein induces complete autophagy through interaction with PYCR2 and down-regulate the expression level of PYCR2, which provide a valuable reference for the role of autophagy during ASFV infection and contribute to the functional clues of PYCR2. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s12250-021-00375-x. Springer Singapore 2021-04-08 /pmc/articles/PMC8027715/ /pubmed/33830435 http://dx.doi.org/10.1007/s12250-021-00375-x Text en © Wuhan Institute of Virology, CAS 2021 |
spellingShingle | Research Article Chen, Sheng Zhang, Xinheng Nie, Yu Li, Hongxin Chen, Weiguo Lin, Wencheng Chen, Feng Xie, Qingmei African Swine Fever Virus Protein E199L Promotes Cell Autophagy through the Interaction of PYCR2 |
title | African Swine Fever Virus Protein E199L Promotes Cell Autophagy through the Interaction of PYCR2 |
title_full | African Swine Fever Virus Protein E199L Promotes Cell Autophagy through the Interaction of PYCR2 |
title_fullStr | African Swine Fever Virus Protein E199L Promotes Cell Autophagy through the Interaction of PYCR2 |
title_full_unstemmed | African Swine Fever Virus Protein E199L Promotes Cell Autophagy through the Interaction of PYCR2 |
title_short | African Swine Fever Virus Protein E199L Promotes Cell Autophagy through the Interaction of PYCR2 |
title_sort | african swine fever virus protein e199l promotes cell autophagy through the interaction of pycr2 |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8027715/ https://www.ncbi.nlm.nih.gov/pubmed/33830435 http://dx.doi.org/10.1007/s12250-021-00375-x |
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