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1-7 of 7
Keywords: RNA polymerase II
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Journal Articles
Journal:
Development
Development (2019) 146 (4): dev167841.
Published: 15 February 2019
... LOCUS C transcription by coupling histone modification and transcription machinery. We demonstrate that TOP1α directly interacts with the methyltransferase SDG8 to establish high levels of H3K36 methylation downstream of FLC transcription start sites and recruits RNA polymerase II to facilitate...
Includes: Supplementary data
Journal Articles
Paul Bardot, Stéphane D. Vincent, Marjorie Fournier, Alexis Hubaud, Mathilde Joint, László Tora, Olivier Pourquié
Journal:
Development
Development (2017) 144 (20): 3808–3818.
Published: 15 October 2017
... the binding of transcription factors to enhancers and promoters. These interactions lead to the assembly of the transcriptional machinery. In non-plant eukaryotes, three RNA polymerases are able to transcribe the genome, among which RNA polymerase II (Pol II) is responsible for the production of mRNA and some...
Includes: Supplementary data
Journal Articles
Liang Chen, Liping Guan, Pingping Qian, Fan Xu, Zhongliang Wu, Yujun Wu, Kai He, Xiaoping Gou, Jia Li, Suiwen Hou
Journal:
Development
Development (2016) 143 (9): 1600–1611.
Published: 1 May 2016
... development have been previously uncovered but much less is known about how signals involved in stomatal development are transmitted to RNA polymerase II (Pol II or RPB), which plays a central role in the transcription of mRNA coding genes. Here, we identify a partial loss-of-function mutation of the third...
Includes: Supplementary data
Journal Articles
Anja Hanisch, Maxine V. Holder, Suma Choorapoikayil, Martin Gajewski, Ertuǧrul M. Özbudak, Julian Lewis
Journal:
Development
Development (2013) 140 (2): 444–453.
Published: 15 January 2013
... and their oscillations have almost identical periods. This is unexpected because the her1 and her7 genes differ greatly in length. We use transgenic zebrafish to measure the RNA polymerase II elongation rate, for the first time, in the intact embryo. This rate is unexpectedly rapid, at 4.8 kb/minute at 28.5°C, implying...
Includes: Multimedia, Supplementary data
Journal Articles
Shrividhya Srinivasan, Jennifer A. Armstrong, Renate Deuring, Ina K. Dahlsveen, Helen McNeill, John W. Tamkun
Journal:
Development
Development (2005) 132 (7): 1623–1635.
Published: 1 April 2005
... salivary gland polytene chromosomes. KIS-L is associated with virtually all sites of transcriptionally active chromatin in a pattern that largely overlaps that of RNA Polymerase II (Pol II). The levels of elongating Pol II and the elongation factors SPT6 and CHD1 are dramatically reduced on polytene...
Journal Articles
Journal:
Development
Development (1997) 124 (11): 2191–2201.
Published: 1 June 1997
... correlates with the absence of a specific phosphoepitope on the carboxyterminal domain of RNA polymerase II. In both C. elegans and Drosophila embryos, this phosphoepitope appears in somatic nuclei coincident with the onset of embryonic transcription, but remains absent from germ cells until these cells...
Journal Articles
Journal:
Development
Development (1995) 121 (8): 2373–2383.
Published: 1 August 1995
... 20 days after birth and reached a plateau around day 40, corresponding to the developmental emergence of haploid cells. Besides TBP, two other components of the general RNA polymerase II machinery, TFIIB and RNA polymerase II, were also overexpressed in testis. By immunostaining, it was found...