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1.
Proc Natl Acad Sci U S A ; 120(36): e2305244120, 2023 09 05.
Artículo en Inglés | MEDLINE | ID: mdl-37639607

RESUMEN

MicroRNAs (miRNAs) play an important role in gene regulation. In Arabidopsis, mature miRNAs are processed from primary miRNA transcripts by the Dicing complex that contains Dicer-like 1 (DCL1), SERRATE (SE), and Hyponastic Leaves 1 (HYL1). The Dicing complex can form nuclear dicing bodies (D-bodies) through SE phase separation. Here, we report that Cyclophilin71 (CYP71), a peptidyl-prolyl isomerase (PPIase), positively regulates miRNA processing. We show that CYP71 directly interacts with SE and enhances its phase separation, thereby promoting the formation of D-body and increasing the activity of the Dicing complex. We further show that the PPIase activity is important for the function of CYP71 in miRNA production. Our findings reveal orchestration of miRNA processing by a cyclophilin protein and suggest the involvement of peptidyl-prolyl cis-trans isomerization, a structural mechanism, in SE phase separation and miRNA processing.


Asunto(s)
Proteínas de Arabidopsis , Arabidopsis , MicroARNs , Arabidopsis/genética , Ciclofilinas/genética , MicroARNs/genética , Hojas de la Planta , Proteínas de Unión al ARN , Proteínas de Arabidopsis/genética
2.
Dev Cell ; 48(3): 371-382.e4, 2019 02 11.
Artículo en Inglés | MEDLINE | ID: mdl-30595534

RESUMEN

As integral regulators in plant development and stress response, microRNAs (miRNAs) themselves need to be tightly regulated. Here, we show that tocopherols (vitamin E), lipid-soluble antioxidants synthesized from tyrosine in chloroplasts, positively regulate the biogenesis of miRNAs. Tocopherols are required for the accumulation of 3'-phosphoadenosine 5'-phosphate (PAP), a retrograde inhibitor of the nuclear exoribonucleases (XRN), which may protect primary miRNAs from being degraded and promote mature miRNA production. Such regulation is involved in heat-induced accumulation of miR398 and plant acquisition of heat tolerance. Our study reveals a chloroplast-to-nucleus signaling mechanism that favors miRNA biogenesis under heat and possibly other environmental perturbations.


Asunto(s)
Arabidopsis/metabolismo , Núcleo Celular/metabolismo , Cloroplastos/metabolismo , MicroARNs/metabolismo , Adenosina Difosfato/metabolismo , Proteínas de Arabidopsis/metabolismo , Exorribonucleasas/metabolismo , Regulación de la Expresión Génica de las Plantas/genética , Transducción de Señal/fisiología , Estrés Fisiológico/fisiología
3.
Plant Cell ; 30(2): 466-480, 2018 02.
Artículo en Inglés | MEDLINE | ID: mdl-29352065

RESUMEN

RNA polymerases IV and V (Pol IV and Pol V) are required for the generation of noncoding RNAs in RNA-directed DNA methylation (RdDM). Their subunit compositions resemble that of Pol II. The mechanism and accessory factors involved in their assembly remain largely unknown. In this study, we identified mutant alleles of MINIYO (IYO), QUATRE-QUART2 (QQT2), and NUCLEAR RNA POLYMERASE B11/D11/E11 (NRPB/D/E11) that cause defects in RdDM in Arabidopsis thaliana We found that Pol IV-dependent small interfering RNAs and Pol V-dependent transcripts were greatly reduced in the mutants. NRPE1, the largest subunit of Pol V, failed to associate with other Pol V subunits in the iyo and qqt2 mutants, suggesting the involvement of IYO and QQT2 in Pol V assembly. In addition, we found that IYO and QQT2 were mutually dependent for their association with the NRPE3 subassembly prior to the assembly of Pol V holoenzyme. Finally, we show that IYO and QQT2 are similarly required for the assembly of Pol II and Pol IV. Our findings reveal IYO and QQT2 as cofactors for the assembly of Pol II, Pol IV, and Pol V and provide mechanistic insights into how RNA polymerases are assembled in plants.


Asunto(s)
Proteínas de Arabidopsis/metabolismo , Arabidopsis/genética , ARN Polimerasas Dirigidas por ADN/metabolismo , GTP Fosfohidrolasas/metabolismo , Factores de Elongación Transcripcional/metabolismo , Alelos , Arabidopsis/enzimología , Arabidopsis/fisiología , Proteínas de Arabidopsis/genética , Metilación de ADN , ARN Polimerasas Dirigidas por ADN/genética , GTP Fosfohidrolasas/genética , Genes Reporteros , Mutación Puntual , ARN Polimerasa II/genética , ARN Polimerasa II/metabolismo , ARN Interferente Pequeño/genética , Factores de Elongación Transcripcional/genética
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