 |
InterPro: IPR008193 DNA-directed RNA polymerase Rpb11, 13-16kDa subunit, conserved site
Protein matches
|
UniProtKB Matches: 341 proteins |
|
Accession
|
IPR008193 RNA_pol_Rpb11_13-16kDa_CS |
Secondary
|
IPR001306
|
Type
|
Conserved_site |
Signatures
|
|
InterPro Relationships
|
|
Found in
|
IPR009025 DNA-directed RNA polymerase, RBP11-like
IPR011261 DNA-directed RNA polymerase, dimerisation
|
GO Term annotation
|
|
Process
|
GO:0006350 transcription
|
|
Function
|
GO:0003677 DNA binding
GO:0003899 DNA-directed RNA polymerase activity
|
|
InterPro annotation
|
|
Entry Details in BioMart
|
Abstract
|
DNA-directed RNA polymerases EC:2.7.7.6 (also known as DNA-dependent RNA polymerases) are responsible for the polymerisation of ribonucleotides into a sequence complementary to the template DNA. In eukaryotes, there are three different forms of DNA-directed RNA polymerases transcribing different sets of genes. Most RNA polymerases are multimeric
enzymes and are composed of a variable number of subunits. The core RNA polymerase complex consists of five subunits (two alpha, one beta, one beta-prime and one omega) and is sufficient for transcription elongation and termination but is unable to initiate transcription. Transcription initiation from promoter elements requires a sixth, dissociable subunit called a sigma factor, which reversibly associates with the core RNA polymerase complex to form a holoenzyme [1]. The core RNA polymerase complex forms a "crab claw"-like structure with an internal channel running along the full length [2]. The key functional sites of the enzyme, as defined by mutational and cross-linking analysis, are located on the inner wall of this channel.
RNA synthesis follows after the attachment of RNA polymerase to a specific site, the promoter, on the template DNA strand. The RNA synthesis process continues until a termination sequence is reached. The RNA product, which is synthesised in the 5' to 3'direction, is known as the primary transcript.
Eukaryotic nuclei contain three distinct types of RNA polymerases that differ in the RNA they synthesise:
- RNA polymerase I: located in the nucleoli, synthesises precursors of most ribosomal RNAs.
- RNA polymerase II: occurs in the nucleoplasm, synthesises mRNA precursors.
- RNA polymerase III: also occurs in the nucleoplasm, synthesises the precursors of 5S ribosomal RNA, the tRNAs, and a variety of other small nuclear and cytosolic RNAs.
Eukaryotic cells are also known to contain separate mitochondrial and chloroplast RNA polymerases. Eukaryotic RNA polymerases, whose molecular masses
vary in size from 500 to 700 kDa, contain two non-identical large (>100 kDa) subunits and an array of up to 12 different small (less than 50 kDa) subunits. In archaea, there is generally a single form of RNA polymerase which also consists of an oligomeric assemblage of 10 to 12 polypeptides. Small subunits of about 13 to 16 kDa are found in all three types of eukaryotic polymerases and in archaeal polymerase. Subunits that belong to this family include: Rpb11 subunit from RNA polymerase II in eukaryotes [3, 4], subunit L from archaeal RNA polymerase [5] and subunit Rpc19 from RNA polymerases I and II in Saccharomyces cerevisiae (Baker's yeast) [6].
|
Structural links
|
|
Database links
|
|
Publications
|
|
1.
|
Helmann JD, Chamberlin MJ.
Structure and function of bacterial sigma factors.
Annu. Rev. Biochem. 57 839-72 1988
[PubMed: 3052291]
http://dx.doi.org/10.1146/annurev.bi.57.070188.004203
|
|
2.
|
Zhang G, Campbell EA, Minakhin L, Richter C, Severinov K, Darst SA.
Crystal structure of Thermus aquaticus core RNA polymerase at 3.3 A resolution.
Cell 98 811-24 1999
[PubMed: 10499798]
http://dx.doi.org/10.1016/S0092-8674(00)81515-9
|
|
3.
|
Woychik NA, McKune K, Lane WS, Young RA.
Yeast RNA polymerase II subunit RPB11 is related to a subunit shared by RNA polymerase I and III.
Gene Expr. 3 77-82 1993
[PubMed: 8508029]
|
|
4.
|
Davis JA, Takagi Y, Kornberg RD, Asturias FA.
Structure of the yeast RNA polymerase II holoenzyme: Mediator conformation and polymerase interaction.
Mol. Cell 10 409-15 2002
[PubMed: 12191485]
http://dx.doi.org/10.1016/S1097-2765(02)00598-1
|
|
5.
|
Reeve JN.
Archaeal chromatin and transcription.
Mol. Microbiol. 48 587-98 2003
[PubMed: 12694606]
http://dx.doi.org/10.1046/j.1365-2958.2003.03439.x
|
|
6.
|
Dequard-Chablat M, Riva M, Carles C, Sentenac A.
RPC19, the gene for a subunit common to yeast RNA polymerases A (I) and C (III).
J. Biol. Chem. 266 15300-7 1991
[PubMed: 1869554]
http://intl.jbc.org/cgi/reprint/266/23/15300.pdf
|
Additional Reading
|
|
Brueckner F, Cramer P.
Structural basis of transcription inhibition by alpha-amanitin and implications for RNA polymerase II translocation.
Nat. Struct. Mol. Biol. 15 2008 811-8
[PubMed: 18552824]
http://dx.doi.org/10.1038/nsmb.1458
|
|
Kaplan CD, Larsson KM, Kornberg RD.
The RNA polymerase II trigger loop functions in substrate selection and is directly targeted by alpha-amanitin.
Mol. Cell 30 2008 547-56
[PubMed: 18538653]
http://dx.doi.org/10.1016/j.molcel.2008.04.023
|
|
Brueckner F, Hennecke U, Carell T, Cramer P.
CPD damage recognition by transcribing RNA polymerase II.
Science 315 2007 859-62
[PubMed: 17290000]
http://dx.doi.org/10.1126/science.1135400
|
|
Lehmann E, Brueckner F, Cramer P.
Molecular basis of RNA-dependent RNA polymerase II activity.
Nature 450 2007 445-9
[PubMed: 18004386]
http://dx.doi.org/10.1038/nature06290
|
|
Damsma GE, Alt A, Brueckner F, Carell T, Cramer P.
Mechanism of transcriptional stalling at cisplatin-damaged DNA.
Nat. Struct. Mol. Biol. 14 2007 1127-33
[PubMed: 17994106]
http://dx.doi.org/10.1038/nsmb1314
|
|
|
InterPro 23.1
|