Literature DB >> 20797633

MMXD, a TFIIH-independent XPD-MMS19 protein complex involved in chromosome segregation.

Shinsuke Ito1, Li Jing Tan, Daisuke Andoh, Takashi Narita, Mineaki Seki, Yasuhiro Hirano, Keiko Narita, Isao Kuraoka, Yasushi Hiraoka, Kiyoji Tanaka.   

Abstract

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. Copyright (c) 2010 Elsevier Inc. All rights reserved.

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Year:  2010        PMID: 20797633     DOI: 10.1016/j.molcel.2010.07.029

Source DB:  PubMed          Journal:  Mol Cell        ISSN: 1097-2765            Impact factor:   17.970


  48 in total

Review 1.  TFIIH: when transcription met DNA repair.

Authors:  Emmanuel Compe; Jean-Marc Egly
Journal:  Nat Rev Mol Cell Biol       Date:  2012-05-10       Impact factor: 94.444

Review 2.  DNA replication, RNAi and epigenetic inheritance.

Authors:  Marlyn Gonzalez; Fei Li
Journal:  Epigenetics       Date:  2012-01-01       Impact factor: 4.528

3.  Plasmodium falciparum XPD translocates in 5' to 3' direction, is expressed throughout the blood stages, and interacts with p44.

Authors:  Leila Tajedin; Mohammed Tarique; Renu Tuteja
Journal:  Protoplasma       Date:  2015-02-24       Impact factor: 3.356

4.  Isomer-specific effect of microRNA miR-29b on nuclear morphology.

Authors:  Alison J Kriegel; Scott S Terhune; Andrew S Greene; Kathleen R Noon; Michael S Pereckas; Mingyu Liang
Journal:  J Biol Chem       Date:  2018-07-13       Impact factor: 5.157

5.  IOP1 protein is an external component of the human cytosolic iron-sulfur cluster assembly (CIA) machinery and functions in the MMS19 protein-dependent CIA pathway.

Authors:  Mineaki Seki; Yukiko Takeda; Kazuhiro Iwai; Kiyoji Tanaka
Journal:  J Biol Chem       Date:  2013-04-12       Impact factor: 5.157

Review 6.  Two steps forward, one step back: determining XPD helicase mechanism by single-molecule fluorescence and high-resolution optical tweezers.

Authors:  Maria Spies
Journal:  DNA Repair (Amst)       Date:  2014-02-21

Review 7.  XPB and XPD helicases in TFIIH orchestrate DNA duplex opening and damage verification to coordinate repair with transcription and cell cycle via CAK kinase.

Authors:  Jill O Fuss; John A Tainer
Journal:  DNA Repair (Amst)       Date:  2011-05-14

8.  ARCH domain of XPD, an anchoring platform for CAK that conditions TFIIH DNA repair and transcription activities.

Authors:  Wassim Abdulrahman; Izarn Iltis; Laura Radu; Cathy Braun; Anne Maglott-Roth; Christophe Giraudon; Jean-Marc Egly; Arnaud Poterszman
Journal:  Proc Natl Acad Sci U S A       Date:  2013-02-04       Impact factor: 11.205

9.  On the traces of XPD: cell cycle matters - untangling the genotype-phenotype relationship of XPD mutations.

Authors:  Elisabetta Cameroni; Karin Stettler; Beat Suter
Journal:  Cell Div       Date:  2010-09-15       Impact factor: 5.130

10.  The mammalian proteins MMS19, MIP18, and ANT2 are involved in cytoplasmic iron-sulfur cluster protein assembly.

Authors:  Niek van Wietmarschen; Annie Moradian; Gregg B Morin; Peter M Lansdorp; Evert-Jan Uringa
Journal:  J Biol Chem       Date:  2012-11-13       Impact factor: 5.157

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