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Molecular and Cellular Biology Volume 25, 2005 - Issue 18
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Chromosome Structure and Dynamics

Transcription-Associated Breaks in Xeroderma Pigmentosum Group D Cells from Patients with Combined Features of Xeroderma Pigmentosum and Cockayne Syndrome

Therina Theron1 Genome Damage and Stability Centre, University of Sussex, Falmer, BrightonBN1 9RQ, United Kingdom
,
Maria I. Fousteri2 MGC Department of Toxicogenetics, Leiden University Medical Centre, Wassenaarseweg 72, 2333AL-Leiden, The Netherlands
,
Marcel Volker1 Genome Damage and Stability Centre, University of Sussex, Falmer, BrightonBN1 9RQ, United Kingdom;2 MGC Department of Toxicogenetics, Leiden University Medical Centre, Wassenaarseweg 72, 2333AL-Leiden, The Netherlands
,
Lorna W. Harries1 Genome Damage and Stability Centre, University of Sussex, Falmer, BrightonBN1 9RQ, United Kingdom
,
Elena Botta3 Istituto di Genetica Molecolare CNR, 27100Pavia, Italy
,
Miria Stefanini3 Istituto di Genetica Molecolare CNR, 27100Pavia, Italy
,
Mitsuo Fujimoto4 Department of Dermatology, Jichi Medical School, Minami-kawachi-machi, Japan
,
Jaan-Olle Andressoo5 MGC Department of Cell Biology and Genetics, P.O. Box 1738, Erasmus University MC, 3000 DRRotterdam, The Netherlands
,
Jay Mitchell5 MGC Department of Cell Biology and Genetics, P.O. Box 1738, Erasmus University MC, 3000 DRRotterdam, The Netherlands
,
Nicolaas G. J. Jaspers5 MGC Department of Cell Biology and Genetics, P.O. Box 1738, Erasmus University MC, 3000 DRRotterdam, The Netherlands
,
Lisa D. McDaniel6 Department of Pathology, CY1.107, UT Southwestern Medical Center, 5323 Harry Hines Blvd., Dallas, Texas75390-8840
,
Leon H. Mullenders2 MGC Department of Toxicogenetics, Leiden University Medical Centre, Wassenaarseweg 72, 2333AL-Leiden, The Netherlands
&
Alan R. Lehmann1 Genome Damage and Stability Centre, University of Sussex, Falmer, BrightonBN1 9RQ, United KingdomCorrespondence[email protected]
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Pages 8368-8378 | Received 07 Mar 2005, Accepted 15 Jun 2005, Published online: 27 Mar 2023

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Mélanie Ferlazzo, Elise Berthel, Adeline Granzotto, Clément Devic, Laurène Sonzogni, Jean-Thomas Bachelet, Sandrine Pereira, Michel Bourguignon, Alain Sarasin, Mauro Mezzina & Nicolas Foray. (2020) Some mutations in the xeroderma pigmentosum D gene may lead to moderate but significant radiosensitivity associated with a delayed radiation-induced ATM nuclear localization. International Journal of Radiation Biology 96:3, pages 394-410.
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G. Huitian, D. Xiuai, Z. Chenglin, W. Xinfeng, L. Yuanyuan, S. Yanan, C. Qihang & X. Huiwen. (2022) Transcriptional Analysis of Listeria monocytogenes Invasion of Macrophages. Applied Biochemistry and Microbiology 58:3, pages 302-308.
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Georgios C Stefos, Eszter Szantai, Dimitris Konstantopoulos, Martina Samiotaki & Maria Fousteri. (2021) aniFOUND: analysing the associated proteome and genomic landscape of the repaired nascent non-replicative chromatin. Nucleic Acids Research 49:11, pages e64-e64.
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Katsuyoshi Horibata, Sayaka Kono, Chie Ishigami, Xue Zhang, Madoka Aizawa, Yuko Kako, Takuma Ishii, Rika Kosaki, Masafumi Saijo & Kiyoji Tanaka. (2015) Constructive rescue of TFIIH instability by an alternative isoform of XPD derived from a mutated XPD allele in mild but not severe XP-D/CS. Journal of Human Genetics 60:5, pages 259-265.
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Emilia Herrera-Moyano, María Moriel-Carretero, Beth A. Montelone & Andrés Aguilera. (2014) The rem Mutations in the ATP-Binding Groove of the Rad3/XPD Helicase Lead to Xeroderma pigmentosum-Cockayne Syndrome-Like Phenotypes. PLoS Genetics 10:12, pages e1004859.
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Dick Jaarsma, Ingrid van der Pluijm, Gijsbertus T.J. van der Horst & Jan H.J. Hoeijmakers. (2013) Cockayne syndrome pathogenesis: Lessons from mouse models. Mechanisms of Ageing and Development 134:5-6, pages 180-195.
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Renier Vélez-Cruz, Anton S. Zadorin, Frédéric Coin & Jean-Marc Egly. (2012) Sirt1 suppresses RNA synthesis after UV irradiation in combined xeroderma pigmentosum group D/Cockayne syndrome (XP-D/CS) cells. Proceedings of the National Academy of Sciences 110:3.
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Marieke van de Ven, Jaan-Olle Andressoo, Gijsbertus T.J. van der Horst, Jan H.J. Hoeijmakers & James R. Mitchell. (2012) Effects of compound heterozygosity at the Xpd locus on cancer and ageing in mouse models. DNA Repair 11:11, pages 874-883.
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María Moriel-Carretero & Andrés Aguilera. (2010) A Postincision-Deficient TFIIH Causes Replication Fork Breakage and Uncovers Alternative Rad51- or Pol32-Mediated Restart Mechanisms. Molecular Cell 37:5, pages 690-701.
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