The C-terminal domain of pol II and a DRB-sensitive kinase are required for 3' processing of U2 snRNA.

The human snRNA genes transcribed by RNA polymerase II (e.g. U1 and U2) have a characteristic TATA-less promoter containing an essential proximal sequence element. Formation of the 3' end of these non-polyadenylated RNAs requires a specialized 3' box element whose function is promoter spec...

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Main Authors: Medlin, J, Uguen, P, Taylor, A, Bentley, D, Murphy, S
Format: Journal article
Language:English
Published: 2003
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author Medlin, J
Uguen, P
Taylor, A
Bentley, D
Murphy, S
author_facet Medlin, J
Uguen, P
Taylor, A
Bentley, D
Murphy, S
author_sort Medlin, J
collection OXFORD
description The human snRNA genes transcribed by RNA polymerase II (e.g. U1 and U2) have a characteristic TATA-less promoter containing an essential proximal sequence element. Formation of the 3' end of these non-polyadenylated RNAs requires a specialized 3' box element whose function is promoter specific. Here we show that truncation of the C-terminal domain (CTD) of RNA polymerase II and treatment of cells with CTD kinase inhibitors, including DRB (5,6-dichloro-1-beta-D-ribofuranosylbenzimidazole), causes a dramatic reduction in proper 3' end formation of U2 transcripts. Activation of 3' box recognition by the phosphorylated CTD would be consistent with the role of phospho-CTD in mRNA processing. CTD kinase inhibitors, however, have little effect on initiation or elongation of transcription of the U2 genes, whereas elongation of transcription of the beta-actin gene is severely affected. This result highlights differences in transcription of snRNA and mRNA genes.
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spelling oxford-uuid:98de6318-0a4f-4548-8b84-30213aa0753e2022-03-27T00:10:02ZThe C-terminal domain of pol II and a DRB-sensitive kinase are required for 3' processing of U2 snRNA.Journal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:98de6318-0a4f-4548-8b84-30213aa0753eEnglishSymplectic Elements at Oxford2003Medlin, JUguen, PTaylor, ABentley, DMurphy, SThe human snRNA genes transcribed by RNA polymerase II (e.g. U1 and U2) have a characteristic TATA-less promoter containing an essential proximal sequence element. Formation of the 3' end of these non-polyadenylated RNAs requires a specialized 3' box element whose function is promoter specific. Here we show that truncation of the C-terminal domain (CTD) of RNA polymerase II and treatment of cells with CTD kinase inhibitors, including DRB (5,6-dichloro-1-beta-D-ribofuranosylbenzimidazole), causes a dramatic reduction in proper 3' end formation of U2 transcripts. Activation of 3' box recognition by the phosphorylated CTD would be consistent with the role of phospho-CTD in mRNA processing. CTD kinase inhibitors, however, have little effect on initiation or elongation of transcription of the U2 genes, whereas elongation of transcription of the beta-actin gene is severely affected. This result highlights differences in transcription of snRNA and mRNA genes.
spellingShingle Medlin, J
Uguen, P
Taylor, A
Bentley, D
Murphy, S
The C-terminal domain of pol II and a DRB-sensitive kinase are required for 3' processing of U2 snRNA.
title The C-terminal domain of pol II and a DRB-sensitive kinase are required for 3' processing of U2 snRNA.
title_full The C-terminal domain of pol II and a DRB-sensitive kinase are required for 3' processing of U2 snRNA.
title_fullStr The C-terminal domain of pol II and a DRB-sensitive kinase are required for 3' processing of U2 snRNA.
title_full_unstemmed The C-terminal domain of pol II and a DRB-sensitive kinase are required for 3' processing of U2 snRNA.
title_short The C-terminal domain of pol II and a DRB-sensitive kinase are required for 3' processing of U2 snRNA.
title_sort c terminal domain of pol ii and a drb sensitive kinase are required for 3 processing of u2 snrna
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