Introduction to mRNA Stability and Localization

RNA is critical at many stages of gene expression. The focus of this chapter is messenger RNA (mRNA), the first RNA to be characterized for its central role as an intermediate in protein synthesis. Many other RNAs play structural or functional roles at other stages of gene expression. The functions of other cellular RNAs are discussed in other chapters: snRNAs and snoRNAs in the chapter titled RNA Splicing and Processing; tRNA and rRNA in the chapter titled Translation; and miRNAs and siRNAs in the chapter titled Regulatory RNA. 
Messenger RNA plays the principal role in the expression of protein-coding genes. Each mRNA molecule carries the genetic code for synthesis of a specific polypeptide during the process of translation. An mRNA carries much more information as well: how frequently it will be translated, how long it is likely to survive, and where in the cell it will be translated. This information is carried in the form of RNA cis-elements and associated proteins. Much of this information is located in parts of the mRNA sequence that are not directly involved in encoding protein.
FIGURE 1 shows some of the structural features typical of mRNAs in prokaryotes and eukaryotes. Bacterial mRNA termini are not modified after transcription, so they begin with the 5′ triphosphate nucleotide used in initiation of transcription and end with the final nucleotide added by RNA polymerase before termination. The 3′ end of many Escherichia coli mRNAs form a hairpin structure involved in intrinsic (rho-independent) transcription termination (see the chapter titled Prokaryotic Transcription).
Eukaryotic mRNAs are cotranscriptionally capped and polyadenylated . Most of the non-protein-coding regulatory information is carried in the 5′ and 3′ untranslated regions (UTRs) of an mRNA, but some elements are present in the coding region. All mRNAs are linear sequences of nucleotides, but secondary and tertiary structures can be formed by intramolecular base pairing.
These structures can be simple, like the stem-loop structures illustrated in Figure 20.1, or more complex, involving branched structures or pairing of nucleotides from distant regions of the molecule. Investigation of the mechanisms by which mRNA regulatory information is deciphered and acted upon by machinery responsible for mRNA degradation, translation, and localization is an important field in molecular biology today.

FIGURE .1 Features of prokaryotic and eukaryotic mRNAs. (a) A typical bacterial mRNA. This is a monocistronic mRNA, but bacterial mRNAs may also be polycistronic. Many bacterial mRNAs end in a terminal stem-loop. (b) All eukaryotic mRNAs begin with a cap (m G), and almost all end with a poly(A) tail. The poly(A) tail is coated with poly(A)-binding proteins (PABPs). Eukaryotic mRNAs may have one or more regions of secondary structure, typically in the 5′ and 3′ UTRs. (c) The major histone mRNAs in mammals have a 3′ terminal stem-loop in place of a poly(A) tail.

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مواضيع ذات صلة

Other Attenuated Systems: Operons, Bacillus subtilis and HIV

Coupling Translation to Termination

trp Multiple Secondary Structures in trp Leader RNA

Early Explorations of the Hypersynthesis

The Serendipitous Discovery of trp Enzyme Hypersynthesis

Rapid Induction Capabilities of the trp Operon

The Aromatic Amino Acid Synthetic Pathway and its Regulation

How AraC Protein Loops and Unloops

DNA Looping and Repression of araBAD

Binding Sites of the ara Regulatory Proteins

Endoplasmic Reticulum-Associated Degradation and the Unfolded Protein Response

Protein Folding and Modifications in the Endoplasmic Reticulum