Eukaryotic RNA Polymerases

Eukaryotes Have Three Nuclear RNA Polymerases Eukaryotic RNA Polymerases Are Not Fully Functional by Themselves... 

Unlike prokaryotes, in which all major types of RNA are synthesized by one RNA polymerase, eukaryotic cells contain three nuclear DNA-dependent RNA polymerases, each responsible for synthesizing a different class of RNAs. 

Eukaryotic RNA polymerases - Eukaryotes contain three distinct RNA polymerases, one each for the synthesis of the three larger rRNAs, mRNA, and small RNAs (tRNA plus the 5S species of rRNA). These are called RNA polymerases I (see here), II (here), and III (here), respectively. The enzymes differ in their sensitivity to inhibition by oi-amanitin (Figure 26.4b), a toxin from the poisonous Amanita mushroom. RNA polymerase II is inhibited at low concentrations, RNA polymerase III is inhibited at high concentrations, and RNA polymerase I is quite resistant. 

The inhibitors of RNA polymerase, which generates RNA from DNA, inhibit a crucial step in gene expression. Inhibition of the eukaryotic form of RNA polymerase is used in cancer chemotherapy and is also an important experimental tool. For example, actinomy-cin D binds to the guanine residues in DNA and blocks the movement of the eukaryotic RNA polymerase. Specific inhibitors of bacterial RNA polymerase can be used as antibacterial agents. Most of these inhibitors like rifamycin bind to the prokaryotic enzyme. 

Consensus sequence in the promoter region of many eukaryotic genes that bind a general transcription factor and hence specifies the position where transcription is initiated by the RNA polymerase. 

The primary transcripts generated by RNA polymerase II—one of three distinct nuclear DNA-depen-dent RNA polymerases in eukaryotes—are promptly capped by 7-methylguanosine triphosphate caps (Figure 35-10) that persist and eventually appear on the 5 end of mature cytoplasmic mRNA. These caps are necessary for the subsequent processing of the primary transcript to mRNA, for the translation of the mRNA, and for protection of the mRNA against exonucleolytic attack. 

One peptide toxin from the mushroom Amanita phalhides, a-amanitin, is a specific differential inhibitor of the eukaryotic nuclear DNA-dependent RNA polymerases and as such has proved to be a powerful research tool (Table 37-2). a-Amanitin blocks the translocation of RNA polymerase during transcription. 

Figure 37-9. The eukaryotic basal transcription complex. Formation of the basal transcription complex begins when TFIID binds to the TATA box. It directs the assembly of several other components by protein-DNA and protein-protein interactions. The entire complex spans DNA from position -30 to +30 relative to the initiation site (+1, marked by bent arrow). The atomic level, x-ray-derived structures of RNA polymerase II alone and ofTBP bound to TATA promoter DNA in the presence of either TFIIB or TFIIA have all been solved at 3 A resolution. The structure of TFIID complexes have been determined by electron microscopy at 30 A resolution. Thus, the molecular structures of the transcription machinery are beginning to be elucidated. Much of this structural information is consistent with the models presented here.

RNA polymerases interact with unique cw-active regions of genes, termed promoters, in order to form preinitiation complexes (PICs) capable of initiation. In eukaryotes the process of PIC formation is facilitated by multiple general transcription factors (GTFs), TFIIA, B, D, E, F, and H. 

Ebright RH RNA polymerase structural similarities between bacterial RNA polymerase and eukaryotic RNA polymerase II. J Mol Biol 2000 304 S87. 

The RNA oligonucleotides are complementary to a sequence on one of the strands of the DNA template and base pair with a portion of the DNA molecule. Subsequently, deoxyribonucleotides are covalently attached to the RNA primer. The synthesis of the primer itself is catalyzed by a special RNA polymerase called primase. Similar RNA polymerase-like enzymes are used to prime the synthesis of certain viral DNAs and eukaryotic DNA. 

A second example of the differences between important biomolecules in archaebacteria and eubacteria is their DNA-dependent RNA polymerase. The enzyme found in archaea resembles that in eukaryotes more than it does those in bacteria ... 

Eukaryotes have a specific signal for termination of transcription however, prokaryotes seem to have lost this mechanism. Once started, RNA polymerase keeps going, making a primary transcript [pre-mRNA or hnRNA (for heterogeneous nuclear)] until far past the end of the final mRNA message. 

Enzyme-stabilized single-stranded DNA (known as the open complex) is the first intermediate formed in transcription initiation of RNA polymerases its formation is the rate-limiting step. Designing molecules which bind specifically to the open complex is a strategy for generating potent transcription inhibitors. The redox-stable complex of Cu(I) with 1,2-dimethyl- 1,10-phenanthroline is an example of such a strategy (405). The Cu(I) complex binds specifically to the single-stranded DNA of transcriptional open complexes and is an effective inhibitor of eukaryotic and prokaryotic transcription. 

Regulation of transcription is a central mechanism by which cells respond to developmental and environmental cues. RNA polymerase Il-mediated transcription in eukaryotes is to a large extent regulated at the level of chromatin, which forms a physical barrier for the binding of proteins to the promoter region of a target gene. The basic unit of chromatin is the nucleosome, which consists of an octamer of histone proteins around which the DNA is wrapped (see Fig. la). 

There are three eukaryotic RNA polymerases, distinguished by the particular types of RNA fhey produce ... 

Transcription factors (such as TFIID for RNA polymerase II) help to initiate transcription. The requirements for termination of transcription in eukaryotes are not well understood. All transcription can be inhibited by actinomycin D. In addition, RNA polymerase II is inhibited by a-amanitin (a toxin from certain mushrooms). These points are summarized in Table 1-3-1,... 

With the help of proteins called transcription factors, RNA polymerase II recognizes and binds to the promoter region. The basal promoter region of eukaryotic genes usually has two consensus sequences called the TATA box (also called Hogness box) and the CAAT box. 

RNA polymerase II ends transcription when it reaches a termination signal. These signals are not well understood in eukaryotes. 

Eukaryotic ribosomal RNA is transcribed in the nucleolus by RNA polymerase I as a single piece of 45S RNA, which is subsequently deaved to yield 28S rRNA, 18S rRNA, and 5.8S rRNA. RNA polymerase III transcribes the 5S rRNA unit from a separate gene. TTie ribosomal subunits assemble in the nudeolus as the rRNA pieces combine with ribosomal proteins. Eukaryotic ribosomal subunits are 60S and 40S. They join during protein synthesis to form the whole SOS ribosome. 

In eukaryotes, general transcription factors must bind to the promoter to allow RNA polymerase II to bind and form the initiation complex at the start site for transcription. General manscription factors are common to most genes. The general transcription factor TFIID (the TATA fector) must bind to the TATA box before RNA polymerase II can bind. Other examples delude SP-1 and NF-.l that modulate basal transcription of many genes. 

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