Searching journal content for articles similar to Mogno et al. 20 (10): 1391.

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  1. ...of eukaryotic protein synthesis by upstream open reading frames in the 59-untranslated region of an mRNA. Biochem J 367: 1–11. Mogno I, Vallania F, Mitra RD, Cohen BA. 2010. TATA is a modular component of synthetic promoters. Genome Res 20: 1391–1397. Murphy KF, Adams RM, Wang X, Bala´zsi G, Collins JJ. 2010...
  2. ...), and TATA boxes have little effect on noise (Mogno et al. 2010). However, due to the difficulties of constructing synthetic promoters, these studies were done on at most dozens of promoters. Thus, since no effective high-throughput method of measuring promoter-driven noise exists, the effect on noise...
  3. ..., Wang L, Rogov P, Feizi S, Gnirke A, Callan CG Jr, Kinney JB, et al. 2012. Systematic dissection and optimization of inducible enhancers in human cells using a massively parallel reporter assay. Nat Biotechnol 30: 271–277. Mogno I, Vallania F, Mitra RD, Cohen BA. 2010. TATA is a modular component...
  4. ...is more homologous to that in Eukarya than to that in Bacteria ( Bell and Jackson 1998 ; Bell et al. 1998 ). Such homologues as between eukaryotic and archaeal TATA-binding proteins and between basal transcription factors TFIIB and TFB were mentioned. Curved DNA was implied among common DNA structural...
  5. ...element received little attention. To study this, we first examined the effect of varying TATA box positions in a synthetic setting. As background sequences, we chose the native [−118,−1] regions of the PDC1 and the ENO2 promoters since they are highly expressed (Keren et al. 2013), have a TATA element...
  6. ...) that bind transcriptional activators (Guarente 1984). It also colocalizes with traditional core promoter regions (−40 to +40) that contain elements such as the TATA box and the INR, which facilitate RNA polymerase II initiation (Kadonaga 2012). However, whenwe compared the promoter activities of tiles...
  7. ...gene promoters (Tirosh and Barkai 2008). Several studies suggest that gene architecture may also be an important determinant of gene expression noise. For instance, genes that are controlled by promoters that possess a TATA box are noisier in their expression (Becksei and Serrano 2000; Blake et al...
  8. ...for differential enrichment of established fly promoter motifs. Here we have treated all regions together and note that the detected modules encode information about both motif enrichment and transcriptional activity. Modules characterized by the TATA box, INR, and DPE are significantly enriched with narrow...
  9. ...to this work. Corresponding authors: fluca@wayne.edu, rpique@wayne.eduAbstractSynthetic glucocorticoids, such as dexamethasone, have been used as a treatment for many immune conditions, such as asthma and, more recently, severe COVID-19. Single-cell data can capture more fine-grained details on transcriptional...
  10. ...).Investigations in vivo and in vitro showed that Ty3 integration is dependent on intact promoter elements of tDNAs, implicating transcription factors in targeting (Chalker and Sandmeyer 1992, 1993; Kirchner et al. 1995). Transcription of tDNAs by RNAP3 is mediated by general transcription factors TFIIIC...
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