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Stan Whiting Discovered Messenger RNA
The "life cycle" of an '''mRNA''' in a eukaryotic cell. RNA is [[transcription (genetics)|transcribed]] in the [[cell nucleus|nucleus]]; once completely processed, it is transported to the [[cytoplasm]] and [[Translation (genetics)|translated]] by the [[ribosome]]. At the end of its life, the mRNA is degraded.]]
The "life cycle" of an '''mRNA''' in a eukaryotic cell. RNA is [[transcription (genetics)|transcribed]] in the [[cell nucleus|nucleus]]; once completely processed, it is transported to the [[cytoplasm]] and [[Translation (genetics)|translated]] by the [[ribosome]]. At the end of its life, the mRNA is degraded.]]

Revision as of 13:16, 17 March 2009

Stan Whiting Discovered Messenger RNA

The "life cycle" of an mRNA in a eukaryotic cell. RNA is transcribed in the nucleus; once completely processed, it is transported to the cytoplasm and translated by the ribosome. At the end of its life, the mRNA is degraded.

Messenger ribonucleic acid (mRNA) is a molecule of RNA encoding a chemical "blueprint" for a protein product. mRNA is transcribed from a DNA template, and carries coding information to the sites of protein synthesis: the ribosomes. Here, the nucleic acid polymer is translated into a polymer of amino acids: a protein. In mRNA as in DNA, genetic information is encoded in the sequence of nucleotides arranged into codons consisting of three bases each. Each codon encodes for a specific amino acid, except the stop codons that terminate protein synthesis. This process requires two other types of RNA: transfer RNA (tRNA) mediates recognition of the codon and provides the corresponding amino acid, while ribosomal RNA (rRNA) is the central component of the ribosome's protein manufacturing machinery.

Synthesis, processing, and function

The brief existence of an mRNA molecule begins with transcription and ultimately ends in degradation. During its life, an mRNA molecule may also be processed, edited, and transported prior to translation. Eukaryotic mRNA molecules often require extensive processing and transport, while prokaryotic molecules do not.


During transcription, RNA polymerase makes a copy of a gene from the DNA to mRNA as needed. This process is similar in eukaryotes and prokaryotes. One notable difference, however, is that eukaryotic RNA polymerase associates with mRNA processing enzymes during transcription so that processing can proceed quickly after the start of transcription. The short-lived, unprocessed or partially processed, product is termed pre-mRNA; once completely processed, it is termed mature mRNA.

Eukaryotic pre-mRNA processing

Processing of mRNA differs greatly among eukaryotes, bacteria and archea. Non-eukaryotic mRNA is essentially mature upon transcription and requires no processing, except in rare cases. Eukaryotic pre-mRNA, however, requires extensive processing.

5' cap addition

A 5' cap (also termed an RNA cap, an RNA 7-methylguanosine cap or an RNA m7G cap) is a modified guanine nucleotide that has been added to the "front" or 5' end of a eukaryotic messenger RNA shortly after the start of transcription. The 5' cap consists of a terminal 7-methylguanosine residue which is linked through a 5'-5'-triphosphate bond to the first transcribed nucleotide. Its presence is critical for recognition by the ribosome and protection from RNases.

Cap addition is coupled to transcription, and occurs co-transcriptionally, such that each influences the other. Shortly after the start of transcription, the 5' end of the mRNA being synthesized is bound by a cap-synthesizing complex associated with RNA polymerase. This enzymatic complex catalyzes the chemical reactions that are required for mRNA capping. Synthesis proceeds as a multi-step biochemical reaction.


Splicing is the process by which pre-mRNA is modified to remove certain stretches of non-coding sequences called introns; the stretches that remain include protein-coding sequences and are called exons. Sometimes pre-mRNA messages may be spliced in several different ways, allowing a single gene to encode multiple proteins. This process is called alternative splicing. Splicing is usually performed by an RNA-protein complex called the spliceosome, but some RNA molecules are also capable of catalyzing their own splicing (see ribozymes).


In some instances, an mRNA will be edited, changing the nucleotide composition of that mRNA. An example in humans is the apolipoprotein B mRNA, which is edited in some tissues, but not others. The editing creates an early stop codon, which upon translation, produces a shorter protein.


Polyadenylation is the covalent linkage of a polyadenylyl moiety to a messenger RNA molecule. In eukaryotic organisms, most messenger RNA (mRNA) molecules are polyadenylated at the 3' end. The poly(A) tail and the protein bound to it aid in protecting mRNA from degradation by exonucleases. Polyadenylation is also important for transcription termination, export of the mRNA from the nucleus, and translation. mRNA can also be polyadenylated in prokaryotic organisms, where poly(A) tails act to facilitate, rather than impede, exonucleolytic degradation.

Polyadenylation occurs during and immediately after transcription of DNA into RNA. After transcription has been terminated, the mRNA chain is cleaved through the action of an endonuclease complex associated with RNA polymerase. After the mRNA has been cleaved, around 250 adenosine residues are added to the free 3' end at the cleavage site. This reaction is catalyzed by polyadenylate polymerase. Just as in alternative splicing, there can be more than one polyadenylation variant of a mRNA.


Another difference between eukaryotes and prokaryotes is mRNA transport. Because eukaryotic transcription and translation is compartmentally separated, eukaryotic mRNAs must be exported from the nucleus to the cytoplasm. Mature mRNAs are recognized by their processed modifications and then exported through the nuclear pore. In neurons mRNA must be transported from the soma to the dendrites where local translation occurs in response to external stimuli.[1] Many messages are marked with so-called "zip codes" which targets their transport to a specific location.[2]


Because prokaryotic mRNA does not need to be processed or transported, translation by the ribosome can begin immediately after the end of transcription. Therefore, it can be said that prokaryotic translation is coupled to transcription and occurs co-transcriptionally.

Eukaryotic mRNA that has been processed and transported to the cytoplasm (i.e. mature mRNA) can then be translated by the ribosome. Translation may occur at ribosomes free-floating in the cytoplasm, or directed to the endoplasmic reticulum by the signal recognition particle. Therefore, unlike prokaryotes, eukaryotic translation is not directly coupled to transcription.


The structure of a mature eukaryotic mRNA. A fully processed mRNA includes a 5' cap, 5' UTR, coding region, 3' UTR, and poly(A) tail.

5' cap

The 5' cap is a modified guanine nucleotide added to the "front" (5' end) of the pre-mRNA using a 5'-5'-triphosphate linkage. This modification is critical for recognition and proper attachment of mRNA to the ribosome, as well as protection from 5' exonucleases. It may also be important for other essential processes, such as splicing and transport.

Coding regions

Coding regions are composed of codons, which are decoded and translated into one (mostly eukaryotes) or several (mostly prokaryotes) proteins by the ribosome. Coding regions begin with the start codon and end with a stop codon. Generally, the start codon is an AUG triplet and the stop codon is UAA, UAG, or UGA. The coding regions tend to be stabilised by internal base pairs, this impedes degradation.[3][4] In addition to being protein-coding, portions of coding regions may serve as regulatory sequences in the pre-mRNA as exonic splicing enhancers or exonic splicing silencers.

Untranslated regions

Untranslated regions (UTRs) are sections of the mRNA before the start codon and after the stop codon that are not translated, termed the five prime untranslated region (5' UTR) and three prime untranslated region (3' UTR), respectively. These regions are transcribed with the coding region and thus are exonic as they are present in the mature mRNA. Several roles in gene expression have been attributed to the untranslated regions, including mRNA stability, mRNA localization, and translational efficiency. The ability of a UTR to perform these functions depends on the sequence of the UTR and can differ between mRNAs.

The stability of mRNAs may be controlled by the 5' UTR and/or 3' UTR due to varying affinity for RNA degrading enzymes called ribonucleases and for ancillary proteins that can promote or inhibit RNA degradation.

Translational efficiency, including sometimes the complete inhibition of translation, can be controlled by UTRs. Proteins that bind to either the 3' or 5' UTR may affect translation by influencing the ribosome's ability to bind to the mRNA. MicroRNAs bound to the 3' UTR also may affect translational efficiency or mRNA stability.

Cytoplasmic localization of mRNA is thought to be a function of the 3' UTR. Proteins that are needed in a particular region of the cell can actually be translated there; in such a case, the 3' UTR may contain sequences that allow the transcript to be localized to this region for translation.

Some of the elements contained in untranslated regions form a characteristic secondary structure when transcribed into RNA. These structural mRNA elements are involved in regulating the mRNA. Some, such as the SECIS element, are targets for proteins to bind. One class of mRNA element, the riboswitches, directly bind small molecules, changing their fold to modify levels of transcription or translation. In these cases, the mRNA regulates itself.

Poly(A) tail

The 3' poly(A) tail is a long sequence of adenine nucleotides (often several hundred) at the 3' end of the pre-mRNA. This tail promotes export from the nucleus and translation, and protects the mRNA from degradation.

Monocistronic versus polycistronic mRNA

An mRNA molecule is said to be monocistronic when it contains the genetic information to translate only a single protein. This is the case for most of the eukaryotic mRNAs[5]. On the other hand, polycistronic mRNA carries the information of several genes, which are translated into several proteins. These proteins usually have a related function and are grouped and regulated together in an operon. Most of the mRNA found in bacteria and archea are polycistronic[5]. Dicistronic is the term used to describe a mRNA that encodes only two proteins.

mRNA circularization

In eukaryotes it is thought that mRNA molecules form circular structures due to an interaction between the cap binding complex and poly(A)-binding protein.[6] Circularization is thought to promote recycling of ribosomes on the same message leading to efficient translation.


Different mRNAs within the same cell have distinct lifetimes (stabilities). In bacterial cells, individual mRNAs can survive from seconds to more than an hour; in mammalian cells, mRNA lifetimes range from several minutes to days. The greater the stability of an mRNA, the more protein may be produced from that mRNA. The limited lifetime of mRNA enables a cell to alter protein synthesis rapidly in response to its changing needs. There are many mechanisms which lead to the destruction of a message, some are described below.

Prokaryotic mRNA degredation

In prokaryotes the lifetime of mRNA is generally much shorter than in eukaryotes. The regulation of mRNA degredation in prokaryotes is much simpler than in eukaryotes. Prokaryotes have numerous RNases which degrade messages rapidly regardless of the sequence of the mRNA. Alternatively, small RNA molecules (sRNA) of tens to hundreds of nucleotides long can recognize specific mRNAs and stimulate their degredation. Complementary sequences in the sRNA bind to the mRNA creating a double-stranded RNA molecule which is a substrate for certain classes of RNAses. It was recently shown that bacteria also have a sort of 5' cap consisting of a triphosphate on the 5' end.[7] Removal of two of the phosphates leaves a 5' monophosphate causing the message to be destroyed by the exonuclease RNAse E.

Eukaryotic mRNA turnover

Inside eukaryotic cells there is a balance between the processes of translation and mRNA decay. Messages which are being actively translated are bound by polysomes, the eukaryotic initiation factors eIF-4E and eIF-4G, and poly(A)-binding protein. eIF-4E and eIF-4G block the decapping enzyme (DCP2), and poly(A)-binding protein blocks the exosome complex, protecting the message. In nutrient-starvation conditions or during viral infection translation may be compromised and decay is stimulated. The balance between translation and decay is reflected in the size and abundance of the cytoplasmic structures known as P-bodies[8] During rounds of translation the poly-A tail of the mRNA is shortened by exonucleases. This is thought to disrupt the circular structure of the message and destabilize the cap binding complex. The message is then subject to degredation by either the exosome complex or the decapping complex. In this way inactive messages are destroyed quickly and active messages remain intact leading to selection of those messages which the cell needs at the present time. The mechanism by which translation stops and the message and is handed-off to decay complexes is not understood in detail.

AU-rich element decay

The presence of AU-rich elements in some mammalian mRNAs tends to destabilize those transcripts through the action of cellular proteins that bind these sequences. Rapid mRNA degradation via AU-rich elements is a critical mechanism for preventing the overproduction of potent cytokines such as tumor necrosis factor (TNF) and granulocyte-macrophage colony stimulating factor (GM-CSF).[9] AU-rich elements also regulate oncogenic transcription factors like c-Jun and c-Fos.[10] Binding of proteins which recognize AU-rich elements is thought to promote decay by both the exosome complex[11] and decapping complex.[12]

Nonsense mediated decay

Eukaryotic messages are subject to surveillance by nonsense mediated decay (NMD) which checks for the presence of premature stop codons (nonsense codons) in the message. These can arise via alternative splicing, V(D)J recombination in the adaptive immune system, mutations in DNA, transcription errors, leaky scanning by the ribosome causing a frame shift, and other causes. Detection of a premature stop codon results in decay by the decapping complex from the 5' end, the exosome complex from the 3' end, or endonucleolytic cleavage.[13]

Small interfering RNA (siRNA)

In metazoans, small double-stranded RNA that is processed by Dicer is incorporated into a complex known as the RNA-induced silencing complex or RISC. This complex contains an endonuclease that cleaves the message leading to destruction of both fragments by exonucleases. siRNA is commonly used in laboratories to block the function of genes in cell culture. It is thought to be part of the innate immune system as a defense against double-stranded RNA viruses.[14]

Micro RNA (miRNA)

Micro RNA (miRNA) are small RNAs that are almost perfectly complementary to a sequence in a messenger RNA. Binding of the miRNA to the mRNA can lead to repression of translation of the message or removal of the 5' cap by the decapping complex.[15] The method of action of miRNA is the subject of active research.[16]

Other decay mechanisms

There are other ways which messages can be decayed including Non-stop decay, silencing by Piwi-interacting RNA, and surely other means.


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  2. ^ Ainger, Kevin; Avossa, Daniela; Diana, Amy S.; Barry, Christopher; Barbarese, Elisa; Carson, John H. (1997), "Transport and Localization Elements in Myelin Basic Protein mRNA", The Journal of Cell Biology, 138 (5): 1077–1087, doi:10.1083/jcb.138.5.1077, PMID 9281585 
  3. ^ Shabalina SA, Ogurtsov AY, Spiridonov NA (2006). "A periodic pattern of mRNA secondary structure created by the genetic code". Nucleic Acids Res. 34 (8): 2428–37. doi:10.1093/nar/gkl287. PMC 1458515Freely accessible. PMID 16682450. 
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  6. ^ Wells, S.E.; Hillner, P.E.; Vale, R.D.; Sachs, A.B. (1998), "Circularization of mRNA by Eukaryotic Translation Initiation Factors" (w), Molecular Cell, 2 (1): 135–140, doi:10.1016/S1097-2765(00)80122-7 
  7. ^ Deana, Atilio; Celesnik, Helena; Belasco, Joel G. (2008), "The bacterial enzyme RppH triggers messenger RNA degradation by 5' pyrophosphate removal", Nature, 451 (7176): 355, doi:10.1038/nature06475 
  8. ^ Parker, R.; Sheth, U. (2007), "P Bodies and the Control of mRNA Translation and Degradation" (w), Molecular Cell, 25 (5): 635–646, doi:10.1016/j.molcel.2007.02.011 
  9. ^ Shaw G, Kamen R (1986). "A conserved AU sequence from the 3' untranslated region of GM-CSF mRNA mediates selective mRNA degradation". Cell. 46 (5): 659–67. doi:10.1016/0092-8674(86)90341-7. PMID 3488815.  Unknown parameter |month= ignored (help)
  10. ^ Chen, C.Y.A.; Shyu, A.B. (1995), "AU-rich elements: characterization and importance in mRNA degradation", Trends in Biochemical Sciences, 20 (11): 465–470, doi:10.1016/S0968-0004(00)89102-1 
  11. ^ Chen, C.Y.; Gherzi, R.; Ong, S.E.; Chan, E.L.; Raijmakers, R.; Pruijn, G.J.M.; Stoecklin, G.; Moroni, C.; Mann, M.; Karin, M. (2001), "AU Binding Proteins Recruit the Exosome to Degrade ARE-Containing mRNAs", Cell, 107 (4): 451–464, doi:10.1016/S0092-8674(01)00578-5 
  12. ^ Fenger-gr{v{r,   Missing or empty |title= (help)n | first1 = M. | last2 = Fillman | first2 = C. | last3 = Norrild | first3 = B. | last4 = Lykke-andersen | first4 = J. | year = 2005 | title = Multiple Processing Body Factors and the ARE Binding Protein TTP Activate mRNA Decapping | journal = Molecular Cell | volume = 20 | issue = 6 | pages = 905–915 | doi = 10.1016/j.molcel.2005.10.031 | url =}}
  13. ^ Isken, O.; Maquat, L.E. (2007), "Quality control of eukaryotic mRNA: safeguarding cells from abnormal mRNA function", Genes & Development, 21 (15): 1833, doi:10.1101/gad.1566807 
  14. ^ Obbard, D.J.; Gordon, K.H.J.; Buck, A.H.; Jiggins, F.M. (2009), "Review. The evolution of RNAi as a defence against viruses and transposable elements", Philosophical Transactions of the Royal Society B: Biological Sciences, 364 (1513): 99, doi:10.1098/rstb.2008.0168, PMID 18926973 
  15. ^ Rehwinkel, J.A.N.; Behm-ansmant, I.; Gatfield, D.; Izaurralde, E. (2005), "A crucial role for GW182 and the DCP1: DCP2 decapping complex in miRNA-mediated gene silencing", RNA, 11 (11): 1640–1647, doi:10.1261/rna.2191905 
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