Phased, Secondary, Small Interfering RNAs in Posttranscriptional Regulatory Networks

被引:394
作者
Fei, Qili [1 ]
Xia, Rui [1 ]
Meyers, Blake C. [1 ]
机构
[1] Univ Delaware, Dept Plant & Soil Sci, Delaware Biotechnol Inst, Newark, DE 19711 USA
基金
美国国家科学基金会;
关键词
TRANS-ACTING SIRNAS; GENOME-WIDE ANALYSIS; DISEASE RESISTANCE GENES; SENSITIVE MALE-STERILITY; NBS-LRR PROTEINS; DNA METHYLATION; ENCODING GENES; NONCODING RNA; DICER-LIKE; ARABIDOPSIS;
D O I
10.1105/tpc.113.114652
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Plant genomes are the source of large numbers of small RNAs, generated via a variety of genetically separable pathways. Several of these pathways converge in the production of phased, secondary, small interfering RNAs (phasiRNAs), originally designated as trans-acting small interfering RNAs or tasiRNAs. PhasiRNA biogenesis requires the involvement of microRNAs as well as the cellular machinery for the production of siRNAs. PhasiRNAs in Arabidopsis thaliana have been well described for their ability to function in trans to suppress target transcript levels. Plant genomic data from an expanding set of species have demonstrated that Arabidopsis is relatively sparing in its use of phasiRNAs, while other genomes contain hundreds or even thousands of phasiRNA-generating loci. In the dicots, targets of those phasiRNAs include several large or conserved families of genes, such as those encoding disease resistance proteins or transcription factors. Suppression of nucleotide-binding, leucine-rich repeat (NB-LRR) disease resistance genes by small RNAs is particularly unusual because of a high level of redundancy. In this review, we discuss plant phasiRNAs and the possible mechanistic significance of phasiRNA-based regulation of the NB-LRRs.
引用
收藏
页码:2400 / 2415
页数:16
相关论文
共 115 条
[1]   DRB4-dependent TAS3 trans-acting siRNAs control leaf morphology through AGO7 [J].
Adenot, Xavier ;
Elmayan, Taline ;
Lauressergues, Dominique ;
Boutet, Stéphanie ;
Bouché, Nicolas ;
Gasciolli, Virginie ;
Vaucheret, Hervé .
CURRENT BIOLOGY, 2006, 16 (09) :927-932
[2]  
Allen E, 2005, CELL, V121, P207, DOI 10.1016/j.cell.2005.04.004
[3]   DICER-LIKE3 Activity in Physcomitrella patens DICER-LIKE4 Mutants Causes Severe Developmental Dysfunction and Sterility [J].
Arif, M. Asif ;
Fattash, Isam ;
Ma, Zhaorong ;
Cho, Sung Hyun ;
Beike, Anna K. ;
Reski, Ralf ;
Axtell, Michael J. ;
Frank, Wolfgang .
MOLECULAR PLANT, 2012, 5 (06) :1281-1294
[4]   Regulation of flowering time and floral organ identity by a microRNA and its APETALA2-like target genes [J].
Aukerman, MJ ;
Sakai, H .
PLANT CELL, 2003, 15 (11) :2730-2741
[5]   A two-hit trigger for siRNA biogenesis in plants [J].
Axtell, Michael J. ;
Jan, Calvin ;
Rajagopalan, Ramya ;
Bartel, David P. .
CELL, 2006, 127 (03) :565-577
[6]   Classification and Comparison of Small RNAs from Plants [J].
Axtell, Michael J. .
ANNUAL REVIEW OF PLANT BIOLOGY, VOL 64, 2013, 64 :137-159
[7]   Initiation of RPS2-specified disease resistance in Arabidopsis is coupled to the AvrRpt2-directed elimination of RIN4 [J].
Axtell, MJ ;
Staskawicz, BJ .
CELL, 2003, 112 (03) :369-377
[8]   Autoimmune response as a mechanism for a Dobzhansky-Muller-type incompatibility syndrome in plants [J].
Bomblies, Kirsten ;
Lempe, Janne ;
Epple, Petra ;
Warthmann, Norman ;
Lanz, Christa ;
Dangl, Jeffery L. ;
Weigel, Detlef .
PLOS BIOLOGY, 2007, 5 (09) :1962-1972
[9]   Hybrid necrosis: autoimmunity as a potential gene-flow barrier in plant species [J].
Bomblies, Kirsten ;
Weigel, Detlef .
NATURE REVIEWS GENETICS, 2007, 8 (05) :382-393
[10]   Endogenous siRNAs derived from a pair of natural cis-antisense transcripts regulate salt tolerance in Arabidopsis [J].
Borsani, O ;
Zhu, JH ;
Verslues, PE ;
Sunkar, R ;
Zhu, JK .
CELL, 2005, 123 (07) :1279-1291