RNA polymerase III

In eukaryote cells, RNA polymerase III (also called Pol III) transcribes DNA to synthesize ribosomal 5S rRNA, tRNA and other small RNAs.

The genes transcribed by RNA Pol III fall in the category of "housekeeping" genes whose expression is required in all cell types and most environmental conditions. Therefore, the regulation of Pol III transcription is primarily tied to the regulation of cell growth and the cell cycle, thus requiring fewer regulatory proteins than RNA polymerase II. Under stress conditions however, the protein Maf1 represses Pol III activity.[1] Rapamycin is another Pol III inhibitor via its direct target TOR.[2]

Transcription

The process of transcription (by any polymerase) involves three main stages:

  • Initiation, requiring construction of the RNA polymerase complex on the gene's promoter
  • Elongation, the synthesis of the RNA transcript
  • Termination, the finishing of RNA transcription and disassembly of the RNA polymerase complex

Initiation

Initiation: the construction of the polymerase complex on the promoter. Pol III is unusual (compared to Pol II) by requiring no control sequences upstream of the gene, instead normally relying on internal control sequences - sequences within the transcribed section of the gene (although upstream sequences are occasionally seen, e.g. U6 snRNA gene has an upstream TATA box as seen in Pol II Promoters).

There are three classes of Pol III initiation, corresponding to 5S rRNA, tRNA, and U6 snRNA initiation. In all cases, the process starts with transcription factors binding to control sequences, and ends with TFIIIB (Transcription Factor for polymerase III B) being recruited to the complex and assembling Pol III. TFIIIB consists of three subunits: TATA binding protein (TBP), a TFIIB-related factor (BRF1, or BRF2 for transcription of a subset of Pol III-transcribed genes in vertebrates), and a B-double-prime (BDP1) unit. The overall architecture bears similarities to that of Pol II.[3]

Class I

Typical stages in 5S rRNA (also termed class I) gene initiation:

  • TFIIIA (Transcription Factor for polymerase III A) binds to the intragenic (lying within the transcribed DNA sequence) 5S rRNA control sequence, the C Block (also termed box C).
  • TFIIIA serves as a platform that replaces the A and B Blocks for positioning TFIIIC in an orientation with respect to the start site of transcription that is equivalent to what is observed for tRNA genes.
  • Once TFIIIC is bound to the TFIIIA-DNA complex, the assembly of TFIIIB proceeds as described for tRNA transcription.

Class II

Typical stages in a tRNA (also termed class II) gene initiation:

  • TFIIIC (Transcription Factor for polymerase III C) binds to two intragenic (lying within the transcribed DNA sequence) control sequences, the A and B Blocks (also termed box A and box B).
  • TFIIIC acts as an assembly factor that positions TFIIIB to bind to DNA at a site centered approximately 26 base pairs upstream of the start site of transcription.
  • TFIIIB is the transcription factor that assembles Pol III at the start site of transcription. Once TFIIIB is bound to DNA, TFIIIC is no longer required. TFIIIB also plays an essential role in promoter opening.

Class III

Typical stages in a U6 snRNA (also termed class III) gene initiation (documented in vertebrates only):

  • SNAPc (SNRNA Activating Protein complex; subunits: 1, 2, 3, 4, 5) (also termed PBP and PTF) binds to the PSE (Proximal Sequence Element) centered approximately 55 base pairs upstream of the start site of transcription. This assembly is greatly stimulated by the Pol II transcription factors Oct1 and STAF that bind to an enhancer-like DSE (Distal Sequence Element) at least 200 base pairs upstream of the start site of transcription. These factors and promoter elements are shared between Pol II and Pol III transcription of snRNA genes.
  • SNAPc acts to assemble TFIIIB at a TATA box centered 26 base pairs upstream of the start site of transcription. It is the presence of a TATA box that specifies that the snRNA gene is transcribed by Pol III rather than Pol II.
  • The TFIIIB for U6 snRNA transcription contains a smaller Brf1 paralogue, Brf2.
  • TFIIIB is the transcription factor that assembles Pol III at the start site of transcription. Sequence conservation predicts that TFIIIB containing Brf2 also plays a role in promoter opening.

Elongation

TFIIIB remains bound to DNA following initiation of transcription by Pol III (unlike bacterial σ factors and most of the basal transcription factors for Pol II transcription). This leads to a high rate of transcriptional reinitiation of Pol III-transcribed genes.

Termination

Polymerase III terminates transcription at small polyTs stretch (5-6). In eukaryotes, a hairpin loop is not required, but may enhance termination efficiency in humans.[4]

Transcribed RNAs

The types of RNAs transcribed from RNA polymerase III include:

See also

References
  1. Vannini, A.; Ringel, R.; Kusser, A. G.; Berninghausen, O.; Kassavetis, G. A.; Cramer, P. (2010). "Molecular Basis of RNA Polymerase III Transcription Repression by Maf1". Cell. 143 (1): 59–70. doi:10.1016/j.cell.2010.09.002. PMID 20887893.
  2. Lee, JaeHoon; Moir, Robyn D.; Willis, Ian M. (2009-05-08). "Regulation of RNA Polymerase III Transcription Involves SCH9-dependent and SCH9-independent Branches of the Target of Rapamycin (TOR) Pathway". Journal of Biological Chemistry. 284 (19): 12604–12608. doi:10.1074/jbc.c900020200. ISSN 0021-9258. PMC 2675989. PMID 19299514.
  3. Han, Y; Yan, C; Fishbain, S; Ivanov, I; He, Y (2018). "Structural visualization of RNA polymerase III transcription machineries". Cell Discovery. 4: 40. doi:10.1038/s41421-018-0044-z. PMC 6066478. PMID 30083386.
  4. Verosloff, M; Corcoran, W; Dolberg, T; Leonard, J; Lucks, J (2020). "RNA sequence and structure determinants of Pol III transcriptional termination in human cells". bioRxiv. doi:10.1101/2020.09.11.294140. S2CID 221713150.
  5. Dieci G, Fiorino G, Castelnuovo M, Teichmann M, Pagano A (December 2007). "The expanding RNA polymerase III transcriptome". Trends Genet. 23 (12): 614–22. doi:10.1016/j.tig.2007.09.001. hdl:11381/1706964. PMID 17977614.
  6. Pagano A, Castelnuovo M, Tortelli F, Ferrari R, Dieci G, Cancedda R (February 2007). "New small nuclear RNA gene-like transcriptional units as sources of regulatory transcripts". PLOS Genet. 3 (2): e1. doi:10.1371/journal.pgen.0030001. PMC 1790723. PMID 17274687.
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