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The In Vivo Kinetics of RNA Polymerase II Elongation during Co-Transcriptional Splicing
by
Neufeld, Noa
, Neugebauer, Karla M.
, Causse, Sebastien Z.
, Shav-Tal, Yaron
, Bieberstein, Nicole
, Böhnlein, Eva-Maria
, Darzacq, Xavier
, Brody, Yehuda
in
beta-Globins - genetics
/ Cell Biology/Gene Expression
/ Cell Biology/Nuclear Structure and Function
/ Experiments
/ Fluorescence Recovery After Photobleaching
/ Gene loci
/ Genetic transcription
/ Genetics
/ Green Fluorescent Proteins - genetics
/ Green Fluorescent Proteins - metabolism
/ Humans
/ Introns
/ Inverted Repeat Sequences
/ Kinetics
/ Lac Repressors - genetics
/ Lac Repressors - metabolism
/ Life sciences
/ Messenger RNA
/ Physiological aspects
/ Proteins
/ Recombinant Fusion Proteins - genetics
/ Recombinant Fusion Proteins - metabolism
/ Ribonucleoproteins, Small Nuclear - genetics
/ Ribonucleoproteins, Small Nuclear - metabolism
/ RNA Polymerase II - metabolism
/ RNA polymerases
/ RNA Precursors - metabolism
/ RNA Splicing
/ RNA, Messenger - metabolism
/ Spliceosomes - metabolism
/ Transcription, Genetic
/ Tumor Cells, Cultured
2011
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The In Vivo Kinetics of RNA Polymerase II Elongation during Co-Transcriptional Splicing
by
Neufeld, Noa
, Neugebauer, Karla M.
, Causse, Sebastien Z.
, Shav-Tal, Yaron
, Bieberstein, Nicole
, Böhnlein, Eva-Maria
, Darzacq, Xavier
, Brody, Yehuda
in
beta-Globins - genetics
/ Cell Biology/Gene Expression
/ Cell Biology/Nuclear Structure and Function
/ Experiments
/ Fluorescence Recovery After Photobleaching
/ Gene loci
/ Genetic transcription
/ Genetics
/ Green Fluorescent Proteins - genetics
/ Green Fluorescent Proteins - metabolism
/ Humans
/ Introns
/ Inverted Repeat Sequences
/ Kinetics
/ Lac Repressors - genetics
/ Lac Repressors - metabolism
/ Life sciences
/ Messenger RNA
/ Physiological aspects
/ Proteins
/ Recombinant Fusion Proteins - genetics
/ Recombinant Fusion Proteins - metabolism
/ Ribonucleoproteins, Small Nuclear - genetics
/ Ribonucleoproteins, Small Nuclear - metabolism
/ RNA Polymerase II - metabolism
/ RNA polymerases
/ RNA Precursors - metabolism
/ RNA Splicing
/ RNA, Messenger - metabolism
/ Spliceosomes - metabolism
/ Transcription, Genetic
/ Tumor Cells, Cultured
2011
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The In Vivo Kinetics of RNA Polymerase II Elongation during Co-Transcriptional Splicing
by
Neufeld, Noa
, Neugebauer, Karla M.
, Causse, Sebastien Z.
, Shav-Tal, Yaron
, Bieberstein, Nicole
, Böhnlein, Eva-Maria
, Darzacq, Xavier
, Brody, Yehuda
in
beta-Globins - genetics
/ Cell Biology/Gene Expression
/ Cell Biology/Nuclear Structure and Function
/ Experiments
/ Fluorescence Recovery After Photobleaching
/ Gene loci
/ Genetic transcription
/ Genetics
/ Green Fluorescent Proteins - genetics
/ Green Fluorescent Proteins - metabolism
/ Humans
/ Introns
/ Inverted Repeat Sequences
/ Kinetics
/ Lac Repressors - genetics
/ Lac Repressors - metabolism
/ Life sciences
/ Messenger RNA
/ Physiological aspects
/ Proteins
/ Recombinant Fusion Proteins - genetics
/ Recombinant Fusion Proteins - metabolism
/ Ribonucleoproteins, Small Nuclear - genetics
/ Ribonucleoproteins, Small Nuclear - metabolism
/ RNA Polymerase II - metabolism
/ RNA polymerases
/ RNA Precursors - metabolism
/ RNA Splicing
/ RNA, Messenger - metabolism
/ Spliceosomes - metabolism
/ Transcription, Genetic
/ Tumor Cells, Cultured
2011
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The In Vivo Kinetics of RNA Polymerase II Elongation during Co-Transcriptional Splicing
Journal Article
The In Vivo Kinetics of RNA Polymerase II Elongation during Co-Transcriptional Splicing
2011
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Overview
RNA processing events that take place on the transcribed pre-mRNA include capping, splicing, editing, 3' processing, and polyadenylation. Most of these processes occur co-transcriptionally while the RNA polymerase II (Pol II) enzyme is engaged in transcriptional elongation. How Pol II elongation rates are influenced by splicing is not well understood. We generated a family of inducible gene constructs containing increasing numbers of introns and exons, which were stably integrated in human cells to serve as actively transcribing gene loci. By monitoring the association of the transcription and splicing machineries on these genes in vivo, we showed that only U1 snRNP localized to the intronless gene, consistent with a splicing-independent role for U1 snRNP in transcription. In contrast, all snRNPs accumulated on intron-containing genes, and increasing the number of introns increased the amount of spliceosome components recruited. This indicates that nascent RNA can assemble multiple spliceosomes simultaneously. Kinetic measurements of Pol II elongation in vivo, Pol II ChIP, as well as use of Spliceostatin and Meayamycin splicing inhibitors showed that polymerase elongation rates were uncoupled from ongoing splicing. This study shows that transcription elongation kinetics proceed independently of splicing at the model genes studied here. Surprisingly, retention of polyadenylated mRNA was detected at the transcription site after transcription termination. This suggests that the polymerase is released from chromatin prior to the completion of splicing, and the pre-mRNA is post-transcriptionally processed while still tethered to chromatin near the gene end.
Publisher
Public Library of Science,Public Library of Science (PLoS)
Subject
/ Cell Biology/Gene Expression
/ Cell Biology/Nuclear Structure and Function
/ Fluorescence Recovery After Photobleaching
/ Genetics
/ Green Fluorescent Proteins - genetics
/ Green Fluorescent Proteins - metabolism
/ Humans
/ Introns
/ Kinetics
/ Proteins
/ Recombinant Fusion Proteins - genetics
/ Recombinant Fusion Proteins - metabolism
/ Ribonucleoproteins, Small Nuclear - genetics
/ Ribonucleoproteins, Small Nuclear - metabolism
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