Abstract
Elongation of RNA polymerase II (Pol II) is thought to be an important mechanism for regulating gene expression [1]. We measured the first wave of de novo transcription in living Drosophila embryos using dual-fluorescence detection of nascent transcripts containing 5′ MS2 and 3′ PP7 RNA stem loops. Pol II elongation rates of 2.4–3.0 kb/min were observed, approximately twice as fast as earlier estimates [2–6]. The revised rates permit substantial levels of zygotic gene activity prior to the mid-blastula transition. We also provide evidence that variable rates of elongation are not a significant source of differential gene activity, suggesting that transcription initiation and Pol II release are the key determinants of gene control in development.
Original language | English (US) |
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Pages (from-to) | 1387-1391 |
Number of pages | 5 |
Journal | Current Biology |
Volume | 27 |
Issue number | 9 |
DOIs | |
State | Published - May 8 2017 |
All Science Journal Classification (ASJC) codes
- General Biochemistry, Genetics and Molecular Biology
- General Agricultural and Biological Sciences
Keywords
- Drosophila embryo
- Pol II elongation
- live imaging
- transcription