Molecular cell · 2010
MMXD, a TFIIH-independent XPD-MMS19 protein complex involved in chromosome segregation.
СтатьяПоддержка исследования: вне правительства СШАНазвание и аннотация: Перевод в очереди
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Ito Shinsuke, Tan Li Jing, Andoh Daisuke, Narita Takashi, Seki Mineaki, Hirano Yasuhiro, Narita Keiko, Kuraoka Isao, Hiraoka Yasushi, Tanaka Kiyoji
Аннотация
Xeroderma pigmentosum group D (XPD) protein is one of the subunits of TFIIH that is required for nucleotide excision repair and transcription. We found a XPD protein complex containing MMS19 that was assumed to be a regulator of TFIIH. However, the MMS19-XPD complex did not contain any other subunits of TFIIH. Instead, it included FAM96B (now designated MIP18), Ciao1, and ANT2. MMS19, MIP18, and XPD localized to the mitotic spindle during mitosis. The siRNA-mediated knockdown of MMS19, MIP18, or XPD led to improper chromosome segregation and the accumulation of nuclei with abnormal shapes. In addition, the frequency of abnormal mitosis and nuclei was increased in XP-D and XP-D/CS patients' cells. These results indicate that the MMS19-XPD protein complex, now designated MMXD (MMS19-MIP18-XPD), is required for proper chromosome segregation, an abnormality of which could contribute to the pathogenesis in some cases of XP-D and XP-D/CS.
Предметные рубрики MeSH
Adenine Nucleotide Translocator 2Binding SitesCarrier ProteinsCell Nucleus ShapeChromosome SegregationGene Knockdown TechniquesHCT116 CellsHeLa CellsHumansMetallochaperonesMetalloproteinsMicroscopy, FluorescenceMitosisMultiprotein ComplexesNuclear ProteinsProtein Interaction Domains and MotifsProtein Interaction MappingRNA InterferenceSpindle ApparatusTranscription Factor TFIIHTranscription FactorsTransfectionXeroderma PigmentosumXeroderma Pigmentosum Group D Protein