The two steps of Poly(A)-dependent termination, pausing and release, can be uncoupled by truncation of the RNA polymerase II carboxyl-terminal repeat domain
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作者:
Park, NJ
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机构:Univ Calif Los Angeles, Dept Chem & Biochem, Los Angeles, CA 90095 USA
Park, NJ
Tsao, DC
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机构:Univ Calif Los Angeles, Dept Chem & Biochem, Los Angeles, CA 90095 USA
Tsao, DC
Martinson, HG
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机构:Univ Calif Los Angeles, Dept Chem & Biochem, Los Angeles, CA 90095 USA
Martinson, HG
机构:
[1] Univ Calif Los Angeles, Dept Chem & Biochem, Los Angeles, CA 90095 USA
[2] Univ Calif Los Angeles, Inst Mol Biol, Los Angeles, CA 90095 USA
The carboxyl-terminal repeat domain (CTD) of RNA polymerase 11 is thought to help coordinate events during RNA metabolism. The mammalian CTD consists of 52 imperfectly repeated heptads followed by 10 additional residues at the C terminus. The CTD is required for cleavage and polyadenylation in vitro. We studied poly(A)-dependent termination in vivo using CTD truncation mutants. Poly(A) -dependent termination occurs in two steps, pause and release. We found that the CTD is required for release, the first 25 heptads being sufficient. Neither the final 10 amino acids nor the variant heptads of the second half of the CTD were required. No part of the CTD was required for poly(A) -dependent pausing-the poly(A) signal could communicate directly with the body of the polymerase. By removing the CTD, pausing could be observed without being obscured by release. Poly (A) -dependent pausing appeared to operate by slowing down the polymerase, such as by down-regulation of a positive elongation factor. Although the first 25 heptads supported undiminished poly(A) -dependent termination, they did not efficiently support events near the promoter involved in abortive elongation. However, the second half of the CTD, including the final 10 amino acids, was sufficient for these functions.
机构:Penn State Univ, Howard Hughes Med Inst, Dept Biochem & Mol Biol, Althouse Lab 306, University Pk, PA 16802 USA
Li, B
Howe, L
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机构:Penn State Univ, Howard Hughes Med Inst, Dept Biochem & Mol Biol, Althouse Lab 306, University Pk, PA 16802 USA
Howe, L
Anderson, S
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机构:Penn State Univ, Howard Hughes Med Inst, Dept Biochem & Mol Biol, Althouse Lab 306, University Pk, PA 16802 USA
Anderson, S
Yates, JR
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机构:Penn State Univ, Howard Hughes Med Inst, Dept Biochem & Mol Biol, Althouse Lab 306, University Pk, PA 16802 USA
Yates, JR
Workman, JL
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Penn State Univ, Howard Hughes Med Inst, Dept Biochem & Mol Biol, Althouse Lab 306, University Pk, PA 16802 USAPenn State Univ, Howard Hughes Med Inst, Dept Biochem & Mol Biol, Althouse Lab 306, University Pk, PA 16802 USA
机构:
Duke Univ, Med Ctr, Dept Mol Genet & Microbiol, Durham, NC 27710 USA
Duke Univ, Med Ctr, Ctr RNA Biol, Durham, NC 27710 USADuke Univ, Med Ctr, Dept Mol Genet & Microbiol, Durham, NC 27710 USA
Natalizio, Barbara J.
Robson-Dixon, Nicole D.
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Duke Univ, Med Ctr, Dept Mol Genet & Microbiol, Durham, NC 27710 USADuke Univ, Med Ctr, Dept Mol Genet & Microbiol, Durham, NC 27710 USA
Robson-Dixon, Nicole D.
Garcia-Blanco, Mariano A.
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Duke Univ, Med Ctr, Dept Mol Genet & Microbiol, Durham, NC 27710 USA
Duke Univ, Med Ctr, Ctr RNA Biol, Durham, NC 27710 USA
Duke Univ, Med Ctr, Dept Med, Durham, NC 27710 USADuke Univ, Med Ctr, Dept Mol Genet & Microbiol, Durham, NC 27710 USA
机构:
Penn State Univ, Ctr Gene Regulat, Dept Biochem & Mol Biol, University Pk, PA 16802 USAPenn State Univ, Ctr Gene Regulat, Dept Biochem & Mol Biol, University Pk, PA 16802 USA
Zhang, ZQ
Wu, CH
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Penn State Univ, Ctr Gene Regulat, Dept Biochem & Mol Biol, University Pk, PA 16802 USAPenn State Univ, Ctr Gene Regulat, Dept Biochem & Mol Biol, University Pk, PA 16802 USA
Wu, CH
Gilmour, DS
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Penn State Univ, Ctr Gene Regulat, Dept Biochem & Mol Biol, University Pk, PA 16802 USAPenn State Univ, Ctr Gene Regulat, Dept Biochem & Mol Biol, University Pk, PA 16802 USA