DCL1

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Endoribonuclease Dicer homolog 1
Cartoon representation of Arabidopsis DCL1 in complex with pri-miRNA 166f. Single chain of DCL1 in light purple catalyzing the cleavage of pri-miRNA-166f into pre-miRNA-166f, before one more cleavage step to finally release miRNA-166f.
Identifiers
OrganismArabidopsis thaliana
SymbolDCL1
Alt. symbolsAT1G01040
PDB7ELD
UniProtQ9SP32
Other data
EC numberEC:3.1.26
Chromosome1: 0.02 - 0.03 Mb
Search for
StructuresSwiss-model
DomainsInterPro

DCL1 (an abbreviation of Dicer-like 1) is a gene in plants that codes for the DCL1 protein, a ribonuclease III enzyme involved in processing double-stranded RNA (dsRNA) and microRNA (miRNA).[1] Although DCL1, also called Endoribonuclease Dicer homolog 1, is named for its homology with the metazoan protein Dicer, its role in miRNA biogenesis is somewhat different, due to substantial differences in miRNA maturation processes between plants and animals,[2] as well due to additional downstream plant-specific pathways, where DCL1 paralogs like DCL4 participate, such Trans-acting siRNA biogenesis.

Function[edit]

DCL1 is localized exclusively in the plant cell nucleus,[3] together with the double-stranded RNA binding protein Hyponastic Leaves1 (HYL1), CTD-Phosphatase-Like1 (CPL1) and the zinc finger protein SERRATE (SE), form nuclear dicing bodies or D-bodies. In these membraneless organelles, pri-miRNAs are recognized and processes into pre-miRNAs and subsequently into mature miRNA duplexes, by the binding of additional proteins such as Constitutive Alterations in the Small RNAs Pathways9 (CARP9).[3] In plants, DCL1 is responsible both for processing a primary miRNA to a pre-miRNA, and for then processing the pre-miRNA to a mature miRNA.[4][5] In animals, the equivalents of these two steps are carried out by different proteins; First, pri-miRNA processing takes place in the nucleus by the ribonuclease Drosha as part of the Microprocessor complex. Second and finally processing to a mature miRNA takes place in the cytoplasm by Dicer to yield a mature miRNA.[2]

PAZ domain plasticity[edit]

A model for DCL1-HYL-SE scaffolding for the pri-miRNA to pre-miRNA maturation process, as well for the pre-miRNA to miRNA maturation step helped by CARP9 binding into the DICER-Complex [3]

In animals, hairpin-containing primary transcripts (pri-miRNAs) are cleaved by Drosha to generate precursor-miRNAs, a double strand palindromic structure typically call hairpin pre-miRNAs, which are subsequently cleaved by Dicer to generate mature miRNAs. Instead of being cleaved by two different enzymes, both cleavages in plants are performed by Dicer-like 1 (DCL1), despite of a similar domain architecuture between both homologgous enzymes.[5] Recent single-particle cryo-electron microscopy structures of both complexs of dsRNA structures (pri-RNA and pre-miRNA) as ligand of Arabidopsis DCL1, in cleavege-competent state, suggest that PAZ domain plasticity allow its to get involved in pri-miRNA and pre-miRNA recognition, posibilited by an internal loop binding groove of this protein domain, which serves as an engine that transfers the substrate between two sequential cleavage events.[5]

Other dicer-like proteins[edit]

Although DCL1 is responsible for the majority of the miRNA processing in plants, most plants contain an additional set of DCLs proteins with related roles in RNA processing,[6] the number of additional members of the same family depends on the plant family. For instance, in Brassicaceae there are 5 additional paralog genes to DLC1, DCL2, DCL3, DCL4 and two RNASE II-LIKE genes RTL1 and RTL2;[7][8] Howeversome dicots such as Populus trichocarpa[9] as well the majority of monocots plants have five to six DCLs, where DCL2 and DCL3 suffered an additional duplication into the genes DCL2a and DCL2. DCL3's duplication is monocot-specifict, generating the genes DCL3a and DCL3b, also called DCL3 and DCL5 respectively.[10][7]

References[edit]

  1. ^ Schauer SE, Jacobsen SE, Meinke DW, Ray A (November 2002). "DICER-LIKE1: blind men and elephants in Arabidopsis development". Trends in Plant Science. 7 (11): 487–491. doi:10.1016/s1360-1385(02)02355-5. PMID 12417148.
  2. ^ a b Axtell MJ, Westholm JO, Lai EC (2011). "Vive la différence: biogenesis and evolution of microRNAs in plants and animals". Genome Biology. 12 (4): 221. doi:10.1186/gb-2011-12-4-221. PMC 3218855. PMID 21554756.
  3. ^ a b c Tomassi AH, Re DA, Romani F, Cambiagno DA, Gonzalo L, Moreno JE, et al. (September 2020). "The Intrinsically Disordered Protein CARP9 Bridges HYL1 to AGO1 in the Nucleus to Promote MicroRNA Activity". Plant Physiology. 184 (1): 316–329. doi:10.1104/pp.20.00258. PMC 7479909. PMID 32636339.
  4. ^ Fang X, Cui Y, Li Y, Qi Y (June 2015). "Transcription and processing of primary microRNAs are coupled by Elongator complex in Arabidopsis". Nature Plants. 1 (6): 15075. doi:10.1038/nplants.2015.75. PMID 27250010. S2CID 12544460.
  5. ^ a b c Wei X, Ke H, Wen A, Gao B, Shi J, Feng Y (October 2021). "Structural basis of microRNA processing by Dicer-like 1". Nature Plants. 7 (10): 1389–1396. doi:10.1038/s41477-021-01000-1. PMID 34593993. S2CID 238240098.
  6. ^ Parent JS, Bouteiller N, Elmayan T, Vaucheret H (January 2015). "Respective contributions of Arabidopsis DCL2 and DCL4 to RNA silencing". The Plant Journal. 81 (2): 223–232. doi:10.1111/tpj.12720. PMID 25376953.
  7. ^ a b Belal MA, Ezzat M, Zhang Y, Xu Z, Cao Y, Han Y (2022). "Integrative Analysis of the DICER-like (DCL) Genes From Peach (Prunus persica): A Critical Role in Response to Drought Stress". Frontiers in Ecology and Evolution. 10. doi:10.3389/fevo.2022.923166. ISSN 2296-701X.
  8. ^ Nagano H, Fukudome A, Hiraguri A, Moriyama H, Fukuhara T (February 2014). "Distinct substrate specificities of Arabidopsis DCL3 and DCL4". Nucleic Acids Research. 42 (3): 1845–1856. doi:10.1093/nar/gkt1077. PMC 3919572. PMID 24214956.
  9. ^ Moura MO, Fausto AK, Fanelli A, Guedes FA, Silva TD, Romanel E, Vaslin MF (November 2019). "Genome-wide identification of the Dicer-like family in cotton and analysis of the DCL expression modulation in response to biotic stress in two contrasting commercial cultivars". BMC Plant Biology. 19 (1): 503. doi:10.1186/s12870-019-2112-4. PMC 6858778. PMID 31729948.
  10. ^ Chen S, Liu W, Naganuma M, Tomari Y, Iwakawa HO (May 2022). "Functional specialization of monocot DCL3 and DCL5 proteins through the evolution of the PAZ domain". Nucleic Acids Research. 50 (8): 4669–4684. doi:10.1093/nar/gkac223. PMC 9071481. PMID 35380679.


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