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{{short description|Enzyme that cleaves double-stranded RNA (dsRNA) into short dsRNA fragments}}
{{Infobox_gene}}

'''Dicer''', also known as '''endoribonuclease Dicer''' or '''helicase with RNase motif''', is an [[enzyme]] that in humans is encoded by the {{gene|DICER1}} [[gene]]. Being part of the [[RNase III]] family, Dicer cleaves [[double-stranded RNA]] (dsRNA) and pre-microRNA (pre-miRNA) into short double-stranded RNA fragments called [[small interfering RNA]] and [[microRNA]], respectively. These fragments are approximately 20–25 [[base pair]]s long with a two-base overhang on the [[Directionality (molecular biology)#3′-end|3′-end]]. Dicer facilitates the activation of the [[RNA-induced silencing complex]] (RISC), which is essential for [[RNA interference]]. RISC has a catalytic component [[Argonaute]], which is an [[endonuclease]] capable of degrading [[messenger RNA]] (mRNA).<ref name="DICER1">{{cite journal | vauthors = Kyriakidis I, Pelagiadis I, Katzilakis N, Stratigaki M, Keklikoglou I, Tragiannidis A, Stiakaki E | title = DICER1 rs3742330 and AGO1 rs636832 polymorphisms and acute lymphoblastic leukemia in Greek children and adolescents: A case-control study | journal = Gene Reports | volume = 37 | issue = December 2024 | article-number = 102043 | date = Sep 2024 | doi = 10.1016/j.genrep.2024.102043 }}</ref>

== Discovery ==

Dicer was given its name in 2001 by [[Stony Brook University|Stony Brook]] PhD student [[Emily Bernstein]] while conducting research in [[Gregory Hannon]]'s lab at [[Cold Spring Harbor Laboratory]]. Bernstein sought to discover the enzyme responsible for generating small RNA fragments from double-stranded RNA. Dicer's ability to generate around 22 nucleotide RNA fragments was discovered by separating it from the RISC enzyme complex after initiating the RNAi pathway with dsRNA [[transfection]]. This experiment showed that RISC was not responsible for generating the observable small nucleotide fragments. Subsequent experiments testing RNase III family enzymes abilities to create RNA fragments narrowed the search to ''[[Drosophila]]'' CG4792, now named Dicer.<ref name=Bernstein_2001>{{cite journal | vauthors = Bernstein E, Caudy AA, Hammond SM, Hannon GJ | title = Role for a bidentate ribonuclease in the initiation step of RNA interference | journal = Nature | volume = 409 | issue = 6818 | pages = 363–6 | year= 2001 | pmid = 11201747 | doi = 10.1038/35053110 | bibcode = 2001Natur.409..363B | s2cid = 4371481 }} {{closed access}}</ref>

Dicer [[Ortholog#Orthology|orthologs]] are present in many other organisms.<ref name="pmid18268840">{{cite book | vauthors = Jaskiewicz L, Filipowicz W | chapter = Role of Dicer in Posttranscriptional RNA Silencing | series = Current Topics in Microbiology and Immunology | title = RNA Interference | volume = 320 | pages = 77–97 | year = 2008 | pmid = 18268840 | doi = 10.1007/978-3-540-75157-1_4 | isbn = 978-3-540-75156-4 }}</ref> In the moss ''[[Physcomitrella patens]]'' DCL1b, one of four DICER proteins, is not involved in miRNA biogenesis but in dicing miRNA target transcripts. Thus, a novel mechanism for [[regulation of gene expression]], the [[epigenetics|epigenetic]] silencing of genes by miRNAs, was discovered.<ref name="pmid20085706">{{cite journal | vauthors = Khraiwesh B, Arif MA, Seumel GI, Ossowski S, Weigel D, [[Ralf Reski|Reski R]], Frank W | title = Transcriptional control of gene expression by microRNAs | journal = Cell | volume = 140 | issue = 1 | pages = 111–22 | date = Jan 2010 | pmid = 20085706 | doi = 10.1016/j.cell.2009.12.023 | doi-access = free }}</ref>

In terms of crystal structure, the first Dicer to be explored was that from the [[protozoan]] ''[[Giardia intestinalis]]''. The work was done by Ian MacRae while conducting research as a postdoctoral fellow in [[Jennifer Doudna]]'s lab at the [[University of California, Berkeley]]. A PAZ domain and two RNase III domains were discovered by [[X-ray crystallography]]. The protein size is 82&nbsp;[[Dalton (unit)|kDa]], representing the conserved functional core that has subsequently been found in larger Dicer proteins in other organisms; for example, it is 219&nbsp;kDa in humans. The difference in size from humans to ''G. intestinalis'' Dicer is due to at least five different domains being present within human Dicer. These domains are important in Dicer activity regulation, dsRNA processing, and RNA interference protein factor functioning.<ref name=Lau>{{cite journal | vauthors = Lau PW, Potter CS, Carragher B, MacRae IJ | title = Structure of the human Dicer-TRBP complex by electron microscopy | journal = Structure | volume = 17 | issue = 10 | pages = 1326–32 | date = Oct 2009 | pmid = 19836333 | pmc = 2880462 | doi = 10.1016/j.str.2009.08.013 }}</ref>

== Functional domains ==
[[File:2ffl-by-domain.png|thumb|200px|left|One molecule of the Dicer protein from ''[[Giardia intestinalis]]'', which catalyzes the cleavage of dsRNA to siRNAs. The [[RNase]] III domains are colored green, the PAZ domain yellow, the platform domain red, and the connector helix blue.<ref name=Macrae_2006>{{cite journal | vauthors = Macrae IJ, Zhou K, Li F, Repic A, Brooks AN, Cande WZ, Adams PD, Doudna JA | title = Structural basis for double-stranded RNA processing by Dicer | journal = Science | volume = 311 | issue = 5758 | pages = 195–8 | date = Jan 2006 | pmid = 16410517 | doi = 10.1126/science.1121638 | bibcode = 2006Sci...311..195M | s2cid = 23785494 }}</ref>]]

Human dicer (also known as hsDicer or [[DICER1]]) is classified a [[Ribonuclease III]] because it cleaves double-stranded RNA. In addition to two RNaseIII domains, it contains a [[helicase]] domain, a PAZ ([[Piwi]]/[[Argonaute]]/Zwille) [[protein domain|domain]],<ref name="entrez">{{cite web | title = Entrez Gene: DICER1 Dicer1, Dcr-1 homolog (Drosophila)| url = https://www.ncbi.nlm.nih.gov/gene?Db=gene&Cmd=ShowDetailView&TermToSearch=23405}}</ref><ref name="pmid10786632">{{cite journal | vauthors = Matsuda S, Ichigotani Y, Okuda T, Irimura T, Nakatsugawa S, Hamaguchi M | title = Molecular cloning and characterization of a novel human gene (HERNA) which encodes a putative RNA-helicase | journal = Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression | volume = 1490 | issue = 1–2 | pages = 163–9 | date = Jan 2000 | pmid = 10786632 | doi = 10.1016/S0167-4781(99)00221-3 }}</ref> and two double stranded RNA binding domains (DUF283 and dsRBD).<ref name=Lau /><ref name = "Hammond_2005">{{cite journal | vauthors = Hammond SM | title = Dicing and slicing: the core machinery of the RNA interference pathway | journal = FEBS Letters | volume = 579 | issue = 26 | pages = 5822–9 | date = Oct 2005 | pmid = 16214139 | doi = 10.1016/j.febslet.2005.08.079 | bibcode = 2005FEBSL.579.5822H | s2cid = 14495726 }}</ref>

Current research suggests the PAZ domain is capable of binding the 2 nucleotide 3' overhang of dsRNA while the RNaseIII catalytic domains form a pseudo-dimer around the dsRNA to initiate cleavage of the strands. This results in a functional shortening of the dsRNA strand. The distance between the PAZ and RNaseIII domains is determined by the angle of the connector helix and influences the length of the micro RNA product.<ref name=Macrae_2006 /> The dsRBD domain binds the dsRNA, although the specific binding site of the domain has not been defined. It is possible that this domain works as part of a complex with other [[regulator protein]]s (TRBP in humans, R2D2, Loqs in ''Drosophila'') in order to effectively position the RNaseIII domains and thus control the specificity of the sRNA products.<ref name=Cenik_2011>{{cite journal | vauthors = Cenik ES, Fukunaga R, Lu G, Dutcher R, Wang Y, Tanaka Hall TM, Zamore PD | title = Phosphate and R2D2 restrict the substrate specificity of Dicer-2, an ATP-driven ribonuclease | journal = Molecular Cell | volume = 42 | issue = 2 | pages = 172–84 | date = Apr 2011 | pmid = 21419681 | pmc = 3115569 | doi = 10.1016/j.molcel.2011.03.002 }}</ref> The helicase domain has been implicated in processing long substrates.<ref name="Cenik_2011"/>

== Role in RNA interference ==

[[File:RNAi-simplified.png|thumb|250px|right|The enzyme dicer trims double stranded RNA or pri-miRNA to form [[small interfering RNA]] or [[microRNA]], respectively. These processed RNAs are incorporated into the [[RNA-induced silencing complex]] (RISC), which targets [[messenger RNA]] to prevent [[translation (genetics)|translation]].<ref name="Hammond2000">{{cite journal | vauthors = Hammond SM, Bernstein E, Beach D, Hannon GJ | title = An RNA-directed nuclease mediates post-transcriptional gene silencing in Drosophila cells | journal = Nature | volume = 404 | issue = 6775 | pages = 293–6 | date = Mar 2000 | pmid = 10749213 | doi = 10.1038/35005107 | bibcode = 2000Natur.404..293H | s2cid = 9091863 }}</ref>]]

===Micro RNA===
[[RNA interference]] is a process where the breakdown of [[RNA]] molecules into [[miRNA]] inhibits [[gene expression]] of specific host mRNA sequences. miRNA is produced within the [[cell (biology)|cell]] starting from primary miRNA (pri-miRNA) in the [[cell nucleus|nucleus]]. These long sequences are cleaved into smaller precursor miRNA (pre-miRNA), which are usually 70 nucleotides with a [[hairpin structure]]. Pri-miRNA are identified by [[DGCR8]] and cleaved by [[Drosha]] to form the pre-miRNA, a process that occurs in the nucleus. These pre-miRNA are then exported to the cytoplasm, where they are cleaved by Dicer to form mature miRNA.<ref name=Merritt>{{cite journal | vauthors = Merritt WM, Bar-Eli M, Sood AK | title = The dicey role of Dicer: implications for RNAi therapy | journal = Cancer Research | volume = 70 | issue = 7 | pages = 2571–4 | date = Apr 2010 | pmid = 20179193 | pmc = 3170915 | doi = 10.1158/0008-5472.CAN-09-2536 }}</ref>

===Small Interfering RNA===
[[Small interfering RNA]] (siRNA) are produced and function in a similar manner to miRNA by cleaving double-stranded RNA with Dicer into smaller fragments, 21 to 23 nucleotides in length.<ref name="Cenik_2011"/> Both miRNAs and siRNAs activate the [[RNA-induced silencing complex]] (RISC), which finds the complementary target mRNA sequence and cleaves the RNA using RNase.<ref name="Vermeulen_2005">{{cite journal | vauthors = Vermeulen A, Behlen L, Reynolds A, Wolfson A, Marshall WS, Karpilow J, Khvorova A | title = The contributions of dsRNA structure to Dicer specificity and efficiency | journal = RNA | volume = 11 | issue = 5 | pages = 674–82 | date = May 2005 | pmid = 15811921 | pmc = 1370754 | doi = 10.1261/rna.7272305 }}</ref>  This in turn silences the particular gene by RNA interference.<ref>{{cite book | author = Watson JD | title = Molecular Biology of the Gene | year = 2008 | publisher = Cold Spring Harbor Laboratory Press | location = San Francisco, CA | isbn = 978-0-8053-9592-1 | pages = 641–648 }}</ref> [[Small interfering RNA|siRNAs]] and [[miRNAs]] differ in the fact that siRNAs are typically specific to the mRNA sequence while miRNAs aren't completely complementary to the mRNA sequence. miRNAs can interact with targets that have similar sequences, which inhibits translation of different genes.<ref name="Zeng_2003">{{cite journal | vauthors = Zeng Y, Yi R, Cullen BR | title = MicroRNAs and small interfering RNAs can inhibit mRNA expression by similar mechanisms | journal = Proceedings of the National Academy of Sciences of the United States of America | volume = 100 | issue = 17 | pages = 9779–84 | date = Aug 2003 | pmid = 12902540 | pmc = 187842 | doi = 10.1073/pnas.1630797100 | bibcode = 2003PNAS..100.9779Z | doi-access = free }}</ref> In general, RNA interference is an essential part of normal processes within organisms such as humans, and it is an area being researched as a diagnostic and therapeutic tool for cancer targets.<ref name=Merritt />

[[File:MiRNA-biogenesis.jpg|thumb|left|x300px|Formation of miRNA used in RNA interference]]

== Disease ==

=== Macular degeneration ===

Age related [[macular degeneration]] is a prominent cause of blindness in developed countries. Dicer's role in this disease became apparent after it was discovered that affected patients showed decreased levels of Dicer in their [[retinal pigment epithelium]] (RPE). Mice with Dicer knocked out, lacking Dicer only in their RPE, exhibited similar symptoms. However, other mice lacking important RNAi pathway proteins like [[Drosha]] and [[Pasha (protein)|Pasha]], did not have symptoms of macular degeneration as Dicer-knockout mice. This observation suggested a Dicer specific role in retinal health that was independent of the RNAi pathway and thus not a function of si/miRNA generation. A form of RNA called Alu RNA (the RNA transcripts of [[alu elements]])) was found to be elevated in patients with insufficient Dicer levels. These non coding strands of RNA can loop forming dsRNA structures that would be degraded by Dicer in a healthy retina. However, with insufficient Dicer levels, the accumulation of alu RNA leads to the degeneration of RPE as a result of inflammation.<ref name="pmid21412326">{{cite journal | vauthors = Meister G | title = Vision: Dicer leaps into view | journal = Nature | volume = 471 | issue = 7338 | pages = 308–9 | date = Mar 2011 | pmid = 21412326 | doi = 10.1038/471308a | bibcode = 2011Natur.471..308M | doi-access = free }}</ref><ref name="pmid22541070">{{cite journal | vauthors = Tarallo V, Hirano Y, Gelfand BD, Dridi S, Kerur N, Kim Y, Cho WG, Kaneko H, Fowler BJ, Bogdanovich S, Albuquerque RJ, Hauswirth WW, Chiodo VA, Kugel JF, Goodrich JA, Ponicsan SL, Chaudhuri G, Murphy MP, Dunaief JL, Ambati BK, Ogura Y, Yoo JW, Lee DK, Provost P, Hinton DR, Núñez G, Baffi JZ, Kleinman ME, Ambati J | title = DICER1 loss and Alu RNA induce age-related macular degeneration via the NLRP3 inflammasome and MyD88 | journal = Cell | volume = 149 | issue = 4 | pages = 847–59 | date = May 2012 | pmid = 22541070 | pmc = 3351582 | doi = 10.1016/j.cell.2012.03.036 }}</ref>

=== Cancer ===

Altered [[miRNA]] expression profiles in malignant cancers suggest a pivotal role of miRNA and thus dicer in cancer development and prognosis. miRNAs can function as tumor suppressors and therefore their altered expression may result in [[tumorigenesis]].<ref name="pmid23222681">{{cite journal | vauthors = Tang KF, Ren H | title = The role of dicer in DNA damage repair | journal = International Journal of Molecular Sciences | volume = 13 | issue = 12 | pages = 16769–78 | year = 2012 | pmid = 23222681 | pmc = 3546719 | doi = 10.3390/ijms131216769 | doi-access = free }}</ref> In analysis of lung and ovarian cancer, poor prognosis and decreased patient survival times correlate with decreased dicer and [[drosha]] expression. Decreased dicer mRNA levels correlate with advanced tumor stage. However, high dicer expression in other cancers, like prostate<ref>{{cite journal | vauthors = Chiosea S, Jelezcova E, Chandran U, Acquafondata M, McHale T, Sobol RW, Dhir R | title = Up-regulation of dicer, a component of the MicroRNA machinery, in prostate adenocarcinoma | journal = The American Journal of Pathology | volume = 169 | issue = 5 | pages = 1812–20 | date = Nov 2006 | pmid = 17071602 | doi = 10.2353/ajpath.2006.060480 | pmc=1780192}}</ref> and esophageal, has been shown to correlate with poor patient prognosis. This discrepancy between cancer types suggests unique RNAi regulatory processes involving dicer differ amongst different tumor types.<ref name=Merritt />

Dicer is also involved in [[DNA repair]]. DNA damage increases in mammalian cells with decreased Dicer expression as a result of decreased efficiency of DNA damage repair and other mechanisms. For example, siRNA from double strand breaks (produced by Dicer) may act as guides for protein complexes involved in the double strand break repair mechanisms and can also direct [[chromatin]] modifications. Additionally, miRNAs expression patterns change as a result of DNA damage caused by ionizing or [[ultraviolet radiation]]. RNAi mechanisms are responsible for [[transposon]] silencing and in their absence, as when Dicer is knocked out/down, can lead to activated transposons that cause DNA damage. Accumulation of DNA damage may result in cells with [[oncogenic]] mutations and thus the development of a tumor.<ref name=Merritt />

=== Other conditions ===

Multinodular [[goiter]] with [[schwannomatosis]] has been shown to be an autosomal dominant condition associated with [[mutation]]s in this gene.<ref name=Rivera2019>Rivera B, Nadaf J, Fahiminiya S, Apellaniz-Ruiz M, Saskin A, Chong AS, Sharma S, Wagener R, Revil T, Condello V, Harra Z, Hamel N, Sabbaghian N, Muchantef K, Thomas C, de Kock L, Hébert-Blouin MN, Bassenden AV, Rabenstein H, Mete O, Paschke R, Pusztaszeri MP, Paulus W, Berghuis A, Ragoussis J, Nikiforov YE, Siebert R, Albrecht S, Turcotte R, Hasselblatt M, Fabian MR, Foulkes WD (2019) DGCR8 microprocessor defect characterizes familial multinodular goiter with schwannomatosis. J Clin Invest </ref>

=== Viral pathogenesis ===

Infection by [[RNA viruses]] can trigger the RNAi cascade. It is likely dicer is involved in viral [[Immunity (medical)|immunity]] as viruses that infect both plant and animal cells contain proteins designed to inhibit the RNAi response. In humans, the viruses [[HIV-1]], [[influenza]], and [[vaccinia]] encode such RNAi suppressing proteins. Inhibition of dicer is beneficial to the virus as dicer is able to cleave viral dsRNA and load the product onto RISC resulting in targeted degradation of viral mRNA; thus fighting the infection. Another potential mechanism for viral pathogenesis is the blockade of dicer as a way to inhibit cellular miRNA pathways.<ref name="pmid16563388">{{cite journal | vauthors = Berkhout B, Haasnoot J | title = The interplay between virus infection and the cellular RNA interference machinery | journal = FEBS Letters | volume = 580 | issue = 12 | pages = 2896–902 | date = May 2006 | pmid = 16563388 | doi = 10.1016/j.febslet.2006.02.070 | pmc = 7094296 | bibcode = 2006FEBSL.580.2896B }}</ref>

=== In insects ===

In ''Drosophila'', Dicer-1 generates microRNAs (miRNAs) by processing pre-miRNA, Dicer-2 is responsible for producing small interfering RNAs (siRNAs) from long double-stranded RNA (dsRNA).<ref>{{cite journal | vauthors = Cenik ES, Fukunaga R, Lu G, Dutcher R, Wang Y, Tanaka Hall TM, Zamore PD | title = Phosphate and R2D2 restrict the substrate specificity of Dicer-2, an ATP-driven ribonuclease | journal = Molecular Cell | volume = 42 | issue = 2 | pages = 172–184 | date = April 2011 | pmid = 21419681 | pmc = 3115569 | doi = 10.1016/j.molcel.2011.03.002 }}</ref>  Insects can use Dicer as a potent [[antiviral protein|antiviral]]. This finding is especially significant given that [[mosquito]]es are responsible for the transmission of many viral diseases including the potentially deadly [[arboviruses]]: [[West Nile virus]], [[dengue fever]] and [[yellow fever]].<ref>{{cite web | publisher = National Center for Infections Disease, Center for Disease Control and Prevention | title = Mosquito-borne Diseases | url = https://www.cdc.gov/ncidod/diseases/list_mosquitoborne.htm | access-date = 22 April 2014 | archive-url = https://web.archive.org/web/20140131004029/http://www.cdc.gov/ncidod/diseases/list_mosquitoborne.htm | archive-date = 31 January 2014 | url-status = dead }}</ref>  While mosquitoes, more specifically the ''[[Aedes aegypti]]'' species, serve as the vectors for these viruses, they are not the intended host of the virus. Transmission occurs as a result of the female mosquito's need for vertebrate blood to develop her eggs. The RNAi pathway in insects is very similar to that of other animals; Dicer-2 cleaves viral RNA and loads it onto the RISC complex where one strand serves as a template for the production of RNAi products and the other is degraded. Insects with mutations leading to non-functional components of their RNAi pathway show increased viral loads for viruses they carry or increased susceptibility to viruses for which they are hosts.  Similarly to humans, insect viruses have evolved mechanisms to avoid the RNAi pathway. As an example, [[Drosophila C virus|''Drosophila C'' virus]] encodes for protein 1A which binds to dsRNA thus protecting it from dicer cleavage as well as RISC loading. ''[[Heliothis virescens]]'' [[ascovirus]] 3a encodes an RNase III enzyme similar to the RNase III domains of dicer which may compete for dsRNA substrate as well as degrade siRNA duplexes to prevent RISC loading.<ref name="pmid24732439">{{cite journal | vauthors = Bronkhorst AW, van Rij RP | title = The long and short of antiviral defense: small RNA-based immunity in insects | journal = Current Opinion in Virology | volume = 7 | pages = 19–28 | date = Aug 2014 | pmid = 24732439 | doi = 10.1016/j.coviro.2014.03.010 }}</ref>

==Diagnostic and therapeutic applications==

Dicer can be used to identify whether [[tumor]]s are present within the body based on the expression level of the enzyme. A study showed that many patients that had [[cancer]] had decreased expression levels of Dicer. The same study showed that lower Dicer expression correlated with lower patient survival length.<ref name=Merritt /> Along with being a [[diagnostic tool]], Dicer can be used for treating patients by injecting foreign siRNA [[intravenous]]ly to cause gene silencing.<ref name="pmid18818708">{{cite journal | vauthors = Kamlah F, Eul BG, Li S, Lang N, Marsh LM, Seeger W, Grimminger F, Rose F, Hänze J | title = Intravenous injection of siRNA directed against hypoxia-inducible factors prolongs survival in a Lewis lung carcinoma cancer model | journal = Cancer Gene Therapy | volume = 16 | issue = 3 | pages = 195–205 | date = Mar 2009 | pmid = 18818708 | doi = 10.1038/cgt.2008.71 | doi-access = free }}</ref>

The siRNA was shown to be delivered in two ways in mammalian species such as mice. One way would be to directly inject into the system, which would not require Dicer function. Another way would be to introduce it by plasmids that encode for short hairpin RNA, which are cleaved by Dicer into siRNA.<ref name=LifeTech>{{cite web|title=Gene silencing by RNA interference is being used routinely to study gene function in cultured mammalian cells|url=http://www.lifetechnologies.com/us/en/home/references/ambion-tech-support/rnai-sirna/tech-notes/performing-rnai-experiments-in-animals.html|work=Life Technologies|access-date=23 April 2014}}</ref>

One of the advantages of using Dicer to produce siRNA therapeutically would be the specificity and diversity of targets it can affect compared to what is currently being used such as [[antibodies]] or [[small molecule|small molecular]] inhibitors. In general, small molecular inhibitors are difficult in terms of specificity along with unendurable side effects. Antibodies are as specific as siRNA, but it is limited by only being able to be used against [[ligand]]s or [[cell surface receptors|surface receptor]]s. On the other hand, low efficiency of [[intracellular]] uptake is the main obstacle of injection of siRNA.<ref name=Merritt /> Injected SiRNA has poor stability in blood and causes stimulations of [[non-specific immunity]].<ref name=Schiffelers>{{cite journal | vauthors = Schiffelers RM, Ansari A, Xu J, Zhou Q, Tang Q, Storm G, Molema G, Lu PY, Scaria PV, Woodle MC | title = Cancer siRNA therapy by tumor selective delivery with ligand-targeted sterically stabilized nanoparticle | journal = Nucleic Acids Research | volume = 32 | issue = 19 | pages = e149 | year = 2004 | pmid = 15520458 | pmc = 528817 | doi = 10.1093/nar/gnh140 }}</ref> Also, producing miRNA therapeutically lacks in specificity because only 6-8 nucleotide base pairing is required for miRNA to attach to mRNA.<ref name="Chi_2009">{{cite journal | vauthors = Chi SW, Zang JB, Mele A, Darnell RB | title = Argonaute HITS-CLIP decodes microRNA-mRNA interaction maps | journal = Nature | volume = 460 | issue = 7254 | pages = 479–86 | date = Jul 2009 | pmid = 19536157 | pmc = 2733940 | doi = 10.1038/nature08170 | bibcode = 2009Natur.460..479C }}</ref>

==Dicer-like proteins==
Plant genomes encode for dicer-like proteins with similar functions and protein domains as animal and insect dicer. For example, in the model organism ''[[Arabidopsis thaliana]]'', four dicer like proteins are made and are designated DCL1 to DCL4. DCL1 is involved with miRNA generation and sRNA production from inverted repeats. DCL2 creates siRNA from [[cis-acting]] antisense transcripts which aid in viral immunity and defense. DCL3 generates siRNA which aids in chromatin modification and DCL4 is involved in [[trans-acting siRNA]] metabolism and transcript silencing at the post-transcriptional level. Additionally, DCL 1 and 3 are important for ''Arabidopsis'' flowering. In ''Arabidopsis'', DCL knockout does not cause severe developmental problems.{{cn|date=August 2025}}

Rice and grapes also produce DCLs as the dicer mechanism is a common defense strategy of many organisms. Rice has evolved other functions for the five DCLs it produces and they play a more important role in function and development than in ''Arabidopsis''. Additionally, expression patterns differ among the different plant cell types of rice while expression in ''Arabidopsis'' is more [[homogeneous]]. Rice DCL expression can be affected by biological stress conditions, including drought, salinity and cold. Thus these stressors may decrease a plant's viral resistance. Unlike ''Arabidopsis'', loss of function of DCL proteins causes developmental defects in rice.<ref>{{cite journal | vauthors = Liu Q, Feng Y, Zhu Z | title = Dicer-like (DCL) proteins in plants | journal = Functional & Integrative Genomics | volume = 9 | issue = 3 | pages = 277–86 | date = Aug 2009 | pmid = 19221817 | doi = 10.1007/s10142-009-0111-5 | s2cid = 28801338 }}</ref>

== See also ==
* [[gene expression]]
* [[RNA-induced silencing complex|RISC]]
* [[RNA interference]]
* [[microRNA]]
* [[Small interfering RNA]]
* [[Drosha]]
* [[Ribonuclease III]]
* [[mRNA]]

== References ==
{{reflist|35em}}

== External links ==
* {{PDBe-KB2|Q9UPY3|Human Endoribonuclease Dicer}}
* {{PDBe-KB2|Q8R418|Mouse Endoribonuclease Dicer}}

{{Esterases}}
{{Enzymes}}
{{Portal bar|Biology|border=no}}

[[Category:Ribonucleases]]
[[Category:RNA interference]]
[[Category:MicroRNA]]
[[Category:EC 3.1.26]]
[[Category:RNA-binding proteins]]