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Five-prime cap

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In molecular biology, the five-prime cap (5′ cap) is a specially altered nucleotide on the 5′ end of some primary transcripts such as precursor messenger RNA. This process, known as mRNA capping, is highly regulated and vital in the creation of stable and mature messenger RNA able to undergo translation during protein synthesis. Mitochondrial mRNA[1] and chloroplastic mRNA[2] are not capped.

Structure

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5′ cap structure (cap-2).
Ribose structure showing the positions of the 2′, 3′ and 5′ carbons.

In eukaryotes, the 5′ cap (cap-0), found on the 5′ end of an mRNA molecule, consists of a guanine nucleotide connected to mRNA via an unusual 5′ to 5′ triphosphate linkage. This guanosine is methylated on the 7 position directly after capping in vivo by a methyltransferase.[3][4][5][6] It is referred to as a 7-methylguanylate cap, abbreviated m7G.

In multicellular eukaryotes and some viruses,[7] further modifications exist, including the methylation of the 2′ hydroxy-groups of the first 2 ribose sugars of the 5′ end of the mRNA. cap-1 has a methylated 2′-hydroxy group on the first ribose sugar, while cap-2 has methylated 2′-hydroxy groups on the first two ribose sugars, shown on the right. The 5′ cap is chemically similar to the 3′ end of an RNA molecule (the 5′ carbon of the cap ribose is bonded, and the 3′ unbonded). This provides significant resistance to 5′ exonucleases.[citation needed]

Small nuclear RNAs contain unique 5′-caps. Sm-class snRNAs are found with 5′-trimethylguanosine caps, while Lsm-class snRNAs are found with 5′-monomethylphosphate caps.[8]

In bacteria, and potentially also in higher organisms, some RNAs are capped with NAD+, NADH, or 3′-dephospho-coenzyme A.[9][10]

In all organisms, mRNA molecules can be decapped in a process known as messenger RNA decapping.

Capping process

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The starting point for capping with 7-methylguanylate is the unaltered 5′ end of an RNA molecule, which terminates at a triphosphate group. This features a final nucleotide followed by three phosphate groups attached to the 5′ carbon.[3] The capping process is initiated before the completion of transcription, as the nascent pre-mRNA is being synthesized.

  1. One of the terminal phosphate groups is removed by RNA triphosphatase, leaving a bisphosphate group (i.e. 5′(ppN)[pN]n);
  2. GTP is added to the terminal bisphosphate by mRNA guanylyltransferase, losing a pyrophosphate from the GTP substrate in the process. This results in the 5′–5′ triphosphate linkage, producing 5′(Gp)(ppN)[pN]n;
  3. The 7-nitrogen of guanine is methylated by mRNA (guanine-N7-)-methyltransferase, with S-adenosyl-L-methionine being demethylated to produce S-adenosyl-L-homocysteine, resulting in 5′(m7Gp)(ppN)[pN]n (cap-0);
  4. Cap-adjacent modifications can occur, normally to the first and second nucleotides, producing up to 5′(m7Gp)(ppN*)(pN*)[pN]n (cap-1 and cap-2);[7]
  5. If the nearest cap-adjacent nucleotide is 2′-O-ribose methyl-adenosine (i.e. 5′(m7Gp)(ppAm)[pN]n), it can be further methylated at the N6 methyl position to form N6-methyladenosine, resulting in 5′(m7Gp)(ppm6Am)[pN]n.[3]

The mechanism of capping with NAD+, NADH, or 3′-dephospho-coenzyme A is different. Capping with NAD+, NADH, or 3′-dephospho-coenzyme A is accomplished through an "ab initio capping mechanism," in which NAD+, NADH, or 3′-desphospho-coenzyme A serves as a "non-canonical initiating nucleotide" (NCIN) for transcription initiation by RNA polymerase and thereby directly is incorporated into the RNA product.[9] Both bacterial RNA polymerase and eukaryotic RNA polymerase II are able to carry out this "ab initio capping mechanism".[9]

Targeting

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For capping with 7-methylguanylate, the capping enzyme complex (CEC) binds to RNA polymerase II before transcription starts. As soon as the 5′ end of the new transcript emerges from RNA polymerase II, the CEC carries out the capping process (this kind of mechanism ensures capping, as with polyadenylation).[11][12][13][14] The enzymes for capping can only bind to RNA polymerase II, ensuring specificity to only these transcripts, which are almost entirely mRNA.[12][14]

Capping with NAD+, NADH, or 3′-dephospho-coenzyme A is targeted by promoter sequence.[9] Capping with NAD+, NADH, or 3′-dephospho-coenzyme A occurs only at promoters that have certain sequences at and immediately upstream of the transcription start site and therefore occurs only for RNAs synthesized from certain promoters.[9]

Function

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The 5′ cap has four main functions:

  1. Regulation of nuclear export;[15][16]
  2. Prevention of degradation by exonucleases;[9][17][18][19]
  3. Promotion of translation (see ribosome and translation);[3][4][5]
  4. Promotion of 5′ proximal intron excision.[20]

Nuclear export of RNA is regulated by the cap binding complex (CBC), which binds exclusively to 7-methylguanylate-capped RNA. The CBC is then recognized by the nuclear pore complex and exported. Once in the cytoplasm after the pioneer round of translation, the CBC is replaced by the translation factors eIF4E and eIF4G of the eIF4F complex.[6] This complex is then recognized by other translation initiation machinery including the ribosome.[21]

Capping with 7-methylguanylate prevents 5′ degradation in two ways. First, degradation of the mRNA by 5′ exonucleases is prevented (as mentioned above) by functionally looking like a 3′ end. Second, the CBC and eIF4E/eIF4G block the access of decapping enzymes to the cap. This increases the half-life of the mRNA, essential in eukaryotes as the export and translation processes take significant time.

Decapping of a 7-methylguanylate-capped mRNA is catalyzed by the decapping complex made up of at least Dcp1 and Dcp2, which must compete with eIF4E to bind the cap. Thus the 7-methylguanylate cap is a marker of an actively translating mRNA and is used by cells to regulate mRNA half-lives in response to new stimuli. Undesirable mRNAs are sent to P-bodies for temporary storage or decapping, the details of which are still being resolved.[22]

The mechanism of 5′ proximal intron excision promotion is not well understood, but the 7-methylguanylate cap appears to loop around and interact with the spliceosome in the splicing process, promoting intron excision.

See also

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References

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  1. ^ Temperley RJ, Wydro M, Lightowlers RN, Chrzanowska-Lightowlers ZM (June 2010). "Human mitochondrial mRNAs—like members of all families, similar but different". Biochimica et Biophysica Acta (BBA) - Bioenergetics. 1797 (6–7): 1081–1085. doi:10.1016/j.bbabio.2010.02.036. PMC 3003153. PMID 20211597.
  2. ^ Monde RA, Schuster G, Stern DB (7 June 2000). "Processing and degradation of chloroplast mRNA". Biochimie. 82 (6–7): 573–582. doi:10.1016/S0300-9084(00)00606-4. PMID 10946108.
  3. ^ a b c d Shatkin, A (December 1976). "Capping of eucaryotic mRNAs". Cell. 9 (4): 645–653. doi:10.1016/0092-8674(76)90128-8. PMID 1017010. S2CID 26743858.
  4. ^ a b Banerjee AK (June 1980). "5′-terminal cap structure in eucaryotic messenger ribonucleic acids". Microbiological Reviews. 44 (2): 175–205. doi:10.1128/mmbr.44.2.175-205.1980. PMC 373176. PMID 6247631.
  5. ^ a b Sonenberg N, Gingras AC (April 1998). "The mRNA 5′ cap-binding protein eIF4E and control of cell growth". Current Opinion in Cell Biology. 10 (2): 268–275. doi:10.1016/S0955-0674(98)80150-6. PMID 9561852.
  6. ^ a b Marcotrigiano J, Gingras AC, Sonenberg N, Burley SK (June 1997). "Cocrystal structure of the messenger RNA 5′ cap-binding protein (eIF4E) bound to 7-methyl-GDP". Cell. 89 (6): 951–961. doi:10.1016/S0092-8674(00)80280-9. PMID 9200613. S2CID 15200116.
  7. ^ a b Fechter P, Brownlee GG (May 2005). "Recognition of mRNA cap structures by viral and cellular proteins". The Journal of General Virology. 86 (Pt 5): 1239–1249. doi:10.1099/vir.0.80755-0. PMID 15831934.
  8. ^ Matera AG, Terns RM, Terns MP (March 2007). "Non-coding RNAs: lessons from the small nuclear and small nucleolar RNAs". Nature Reviews. Molecular Cell Biology. 8 (3): 209–220. doi:10.1038/nrm2124. PMID 17318225. S2CID 30268055.
  9. ^ a b c d e f Bird JG, Zhang Y, Tian Y, Panova N, Barvík I, Greene L, Liu M, Buckley B, Krásný L, Lee JK, Kaplan CD, Ebright RH, Nickels BE (July 2016). "The mechanism of RNA 5′ capping with NAD+, NADH and desphospho-CoA". Nature. 535 (7612): 444–447. Bibcode:2016Natur.535..444B. doi:10.1038/nature18622. PMC 4961592. PMID 27383794.
  10. ^ Cahová H, Winz ML, Höfer K, Nübel G, Jäschke A (March 2015). "NAD captureSeq indicates NAD as a bacterial cap for a subset of regulatory RNAs". Nature. 519 (7543): 374–377. Bibcode:2015Natur.519..374C. doi:10.1038/nature14020. PMID 25533955. S2CID 4446837.
  11. ^ Cho EJ, Takagi T, Moore CR, Buratowski S (December 1997). "mRNA capping enzyme is recruited to the transcription complex by phosphorylation of the RNA polymerase II carboxy-terminal domain". Genes & Development. 11 (24): 3319–3326. doi:10.1101/gad.11.24.3319. PMC 316800. PMID 9407025.
  12. ^ a b Fabrega C, Shen V, Shuman S, Lima CD (June 2003). "Structure of an mRNA capping enzyme bound to the phosphorylated carboxy-terminal domain of RNA polymerase II". Molecular Cell. 11 (6): 1549–1561. doi:10.1016/S1097-2765(03)00187-4. PMID 12820968.
  13. ^ Ho CK, Lehman K, Shuman S (December 1999). "An essential surface motif (WAQKW) of yeast RNA triphosphatase mediates formation of the mRNA capping enzyme complex with RNA guanylyltransferase". Nucleic Acids Research. 27 (24): 4671–4678. doi:10.1093/nar/27.24.4671. PMC 148765. PMID 10572165.
  14. ^ a b Hirose Y, Manley JL (June 2000). "RNA polymerase II and the integration of nuclear events". Genes & Development. 14 (12): 1415–1429. doi:10.1101/gad.14.12.1415. PMID 10859161. S2CID 43589702. Retrieved 23 November 2014.
  15. ^ Visa N, Izaurralde E, Ferreira J, Daneholt B, Mattaj IW (April 1996). "A nuclear cap-binding complex binds Balbiani ring pre-mRNA cotranscriptionally and accompanies the ribonucleoprotein particle during nuclear export". The Journal of Cell Biology. 133 (1): 5–14. doi:10.1083/jcb.133.1.5. PMC 2120770. PMID 8601613.
  16. ^ Lewis JD, Izaurralde E (July 1997). "The role of the cap structure in RNA processing and nuclear export". European Journal of Biochemistry. 247 (2): 461–469. doi:10.1111/j.1432-1033.1997.00461.x. PMID 9266685.
  17. ^ Evdokimova V, Ruzanov P, Imataka H, Raught B, Svitkin Y, Ovchinnikov LP, Sonenberg N (October 2001). "The major mRNA-associated protein YB-1 is a potent 5′ cap-dependent mRNA stabilizer". The EMBO Journal. 20 (19): 5491–5502. doi:10.1093/emboj/20.19.5491. PMC 125650. PMID 11574481.
  18. ^ Gao M, Fritz DT, Ford LP, Wilusz J (March 2000). "Interaction between a poly(A)-specific ribonuclease and the 5′ cap influences mRNA deadenylation rates in vitro". Molecular Cell. 5 (3): 479–488. doi:10.1016/S1097-2765(00)80442-6. PMC 2811581. PMID 10882133.
  19. ^ Burkard KT, Butler JS (January 2000). "A nuclear 3′–5′ exonuclease involved in mRNA degradation interacts with Poly(A) polymerase and the hnRNA protein Npl3p". Molecular and Cellular Biology. 20 (2): 604–616. doi:10.1128/MCB.20.2.604-616.2000. PMC 85144. PMID 10611239.
  20. ^ Konarska MM, Padgett RA, Sharp PA (October 1984). "Recognition of cap structure in splicing in vitro of mRNA precursors". Cell. 38 (3): 731–736. doi:10.1016/0092-8674(84)90268-X. PMID 6567484. S2CID 10721149.
  21. ^ Kapp LD, Lorsch JR (2004). "The molecular mechanics of eukaryotic translation". Annual Review of Biochemistry. 73 (1): 657–704. doi:10.1146/annurev.biochem.73.030403.080419. PMID 15189156.
  22. ^ Parker R, Sheth U (March 2007). "P bodies and the control of mRNA translation and degradation". Molecular Cell. 25 (5): 635–646. doi:10.1016/j.molcel.2007.02.011. PMID 17349952.
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  • "RNA Caps". PubMed Medical Subject Heading (MeSH). National Institutes of Health.
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