Academic Journal

CTCF interacts with the lytic HSV-1 genome to promote viral transcription

التفاصيل البيبلوغرافية
العنوان: CTCF interacts with the lytic HSV-1 genome to promote viral transcription
المؤلفون: Lang, Fengchao, Li, Xin, Vladimirova, Olga, Hu, Benxia, Chen, Guijun, Xiao, Yu, Singh, Vikrant, Lu, Danfeng, Li, Lihong, Han, Hongbo, Wickramasinghe, J. M. A. S. P., Smith, Sheryl T., Zheng, Chunfu, Li, Qihan, Lieberman, Paul M., Fraser, Nigel W., Zhou, Jumin
المصدر: Scientific Reports ; volume 7, issue 1 ; ISSN 2045-2322
بيانات النشر: Springer Science and Business Media LLC
سنة النشر: 2017
الوصف: CTCF is an essential chromatin regulator implicated in important nuclear processes including in nuclear organization and transcription. Herpes Simplex Virus-1 (HSV-1) is a ubiquitous human pathogen, which enters productive infection in human epithelial and many other cell types. CTCF is known to bind several sites in the HSV-1 genome during latency and reactivation, but its function has not been defined. Here, we report that CTCF interacts extensively with the HSV-1 DNA during lytic infection by ChIP-seq, and its knockdown results in the reduction of viral transcription, viral genome copy number and virus yield. CTCF knockdown led to increased H3K9me3 and H3K27me3, and a reduction of RNA pol II occupancy on viral genes. Importantly, ChIP-seq analysis revealed that there is a higher level of CTD Ser2P modified RNA Pol II near CTCF peaks relative to the Ser5P form in the viral genome. Consistent with this, CTCF knockdown reduced the Ser2P but increased Ser5P modified forms of RNA Pol II on viral genes. These results suggest that CTCF promotes HSV-1 lytic transcription by facilitating the elongation of RNA Pol II and preventing silenced chromatin on the viral genome.
نوع الوثيقة: article in journal/newspaper
اللغة: English
DOI: 10.1038/srep39861
الاتاحة: http://dx.doi.org/10.1038/srep39861
https://www.nature.com/articles/srep39861.pdf
https://www.nature.com/articles/srep39861
Rights: https://creativecommons.org/licenses/by/4.0 ; https://creativecommons.org/licenses/by/4.0
رقم الانضمام: edsbas.EA9B5589
قاعدة البيانات: BASE