The structural basis of localizing polo-like kinase to the flagellum attachment zone in Trypanosoma brucei.
The polo-like kinase in the deep branching eukaryote Trypanosoma brucei (TbPlk) has many unique features. Unlike all the other polo-like kinases known to associate with the nucleus and controlling both mitosis and cytokinesis, TbPlk localizes to the flagellum attachment zone (FAZ) and regulates only...
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| Format: | Article |
| Language: | English |
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Public Library of Science (PLoS)
2011-01-01
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| Series: | PLoS ONE |
| Online Access: | http://europepmc.org/articles/PMC3214037?pdf=render |
| _version_ | 1819019566221623296 |
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| author | Lu Sun Ching C Wang |
| author_facet | Lu Sun Ching C Wang |
| author_sort | Lu Sun |
| collection | DOAJ |
| description | The polo-like kinase in the deep branching eukaryote Trypanosoma brucei (TbPlk) has many unique features. Unlike all the other polo-like kinases known to associate with the nucleus and controlling both mitosis and cytokinesis, TbPlk localizes to the flagellum attachment zone (FAZ) and regulates only cytokinesis in T. brucei. TbPlk was, however, previously found capable of complementing all the multiple Plk (Cdc5) functions in Saccharomyces cerevisiae, indicating that it has acquired all the functions of Cdc5. In the present study, Cdc5 tagged with an enhanced yellow fluorescence protein (EYFP) localized exclusively in the FAZ of T. brucei, suggesting that the unusual localization and limited function of TbPlk are probably attributed to the particular environment in T. brucei cells. Structural basis for the FAZ localization of TbPlk was further investigated with TbPlk and TbPlk mutants tagged with EYFP and expressed in T. brucei. The results indicated that a kinase-inactive mutant N169A and a TbPlk mutant with the entire kinase domain (KD) deleted both localized to the FAZ. Substantial association with FAZ was also maintained when one of the two polo-boxes (PB1 or 2) or the linker region between them was deleted from TbPlk. But a deletion of both polo-boxes led to a complete exclusion of the protein from FAZ. All the deletion mutants retained the kinase activity, further indicating that the TbPlk kinase function does not play a role for FAZ localization. The two polo boxes in TbPlk are most likely instrumental in localizing the protein to FAZ through potential interactions with certain FAZ structural component(s). A putative cryptic bipartite nuclear targeting signal was identified in TbPlk, which was capable of directing TbPlk into the nucleus when either the kinase activity was lost or the PB1 was deleted from the protein. |
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| id | doaj.art-aa5e3ab4efec4605a4894b221ccf5617 |
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| language | English |
| last_indexed | 2024-12-21T03:37:21Z |
| publishDate | 2011-01-01 |
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| spelling | doaj.art-aa5e3ab4efec4605a4894b221ccf56172022-12-21T19:17:19ZengPublic Library of Science (PLoS)PLoS ONE1932-62032011-01-01611e2730310.1371/journal.pone.0027303The structural basis of localizing polo-like kinase to the flagellum attachment zone in Trypanosoma brucei.Lu SunChing C WangThe polo-like kinase in the deep branching eukaryote Trypanosoma brucei (TbPlk) has many unique features. Unlike all the other polo-like kinases known to associate with the nucleus and controlling both mitosis and cytokinesis, TbPlk localizes to the flagellum attachment zone (FAZ) and regulates only cytokinesis in T. brucei. TbPlk was, however, previously found capable of complementing all the multiple Plk (Cdc5) functions in Saccharomyces cerevisiae, indicating that it has acquired all the functions of Cdc5. In the present study, Cdc5 tagged with an enhanced yellow fluorescence protein (EYFP) localized exclusively in the FAZ of T. brucei, suggesting that the unusual localization and limited function of TbPlk are probably attributed to the particular environment in T. brucei cells. Structural basis for the FAZ localization of TbPlk was further investigated with TbPlk and TbPlk mutants tagged with EYFP and expressed in T. brucei. The results indicated that a kinase-inactive mutant N169A and a TbPlk mutant with the entire kinase domain (KD) deleted both localized to the FAZ. Substantial association with FAZ was also maintained when one of the two polo-boxes (PB1 or 2) or the linker region between them was deleted from TbPlk. But a deletion of both polo-boxes led to a complete exclusion of the protein from FAZ. All the deletion mutants retained the kinase activity, further indicating that the TbPlk kinase function does not play a role for FAZ localization. The two polo boxes in TbPlk are most likely instrumental in localizing the protein to FAZ through potential interactions with certain FAZ structural component(s). A putative cryptic bipartite nuclear targeting signal was identified in TbPlk, which was capable of directing TbPlk into the nucleus when either the kinase activity was lost or the PB1 was deleted from the protein.http://europepmc.org/articles/PMC3214037?pdf=render |
| spellingShingle | Lu Sun Ching C Wang The structural basis of localizing polo-like kinase to the flagellum attachment zone in Trypanosoma brucei. PLoS ONE |
| title | The structural basis of localizing polo-like kinase to the flagellum attachment zone in Trypanosoma brucei. |
| title_full | The structural basis of localizing polo-like kinase to the flagellum attachment zone in Trypanosoma brucei. |
| title_fullStr | The structural basis of localizing polo-like kinase to the flagellum attachment zone in Trypanosoma brucei. |
| title_full_unstemmed | The structural basis of localizing polo-like kinase to the flagellum attachment zone in Trypanosoma brucei. |
| title_short | The structural basis of localizing polo-like kinase to the flagellum attachment zone in Trypanosoma brucei. |
| title_sort | structural basis of localizing polo like kinase to the flagellum attachment zone in trypanosoma brucei |
| url | http://europepmc.org/articles/PMC3214037?pdf=render |
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