Literature DB >> 30020552

Reproductive phasiRNAs in grasses are compositionally distinct from other classes of small RNAs.

Parth Patel1,2, Sandra Mathioni2,3, Atul Kakrana1,2, Hagit Shatkay1,2,4, Blake C Meyers3,5.   

Abstract

Little is known about the characteristics and function of reproductive phased, secondary, small interfering RNAs (phasiRNAs) in the Poaceae, despite the availability of significant genomic resources, experimental data, and a growing number of computational tools. We utilized machine-learning methods to identify sequence-based and positional features that distinguish phasiRNAs in rice and maize from other small RNAs (sRNAs). We developed Random Forest classifiers that can distinguish reproductive phasiRNAs from other sRNAs in complex sets of sequencing data, utilizing sequence-based (k-mers) and features describing position-specific sequence biases. The classification performance attained is > 80% in accuracy, sensitivity, specificity, and positive predicted value. Feature selection identified important features in both ends of phasiRNAs. We demonstrated that phasiRNAs have strand specificity and position-specific nucleotide biases potentially influencing AGO sorting; we also predicted targets to infer functions of phasiRNAs, and computationally assessed their sequence characteristics relative to other sRNAs. Our results demonstrate that machine-learning methods effectively identify phasiRNAs despite the lack of characteristic features typically present in precursor loci of other small RNAs, such as sequence conservation or structural motifs. The 5'-end features we identified provide insights into AGO-phasiRNA interactions. We describe a hypothetical model of competition for AGO loading between phasiRNAs of different nucleotide compositions.
© 2018 The Authors. New Phytologist © 2018 New Phytologist Trust.

Entities:  

Keywords:  P4-siRNAs; classification; feature selection; heterochromatic siRNAs; machine learning; miRNAs; plant small RNAs; reproductive phasiRNAs

Mesh:

Substances:

Year:  2018        PMID: 30020552     DOI: 10.1111/nph.15349

Source DB:  PubMed          Journal:  New Phytol        ISSN: 0028-646X            Impact factor:   10.151


  10 in total

Review 1.  PhasiRNAs in Plants: Their Biogenesis, Genic Sources, and Roles in Stress Responses, Development, and Reproduction.

Authors:  Yuanlong Liu; Chong Teng; Rui Xia; Blake C Meyers
Journal:  Plant Cell       Date:  2020-08-18       Impact factor: 11.277

Review 2.  Plant Noncoding RNAs: Hidden Players in Development and Stress Responses.

Authors:  Yu Yu; Yuchan Zhang; Xuemei Chen; Yueqin Chen
Journal:  Annu Rev Cell Dev Biol       Date:  2019-08-12       Impact factor: 13.827

3.  A cascade of bHLH-regulated pathways programs maize anther development.

Authors:  Guo-Ling Nan; Chong Teng; John Fernandes; Lily O'Connor; Blake C Meyers; Virginia Walbot
Journal:  Plant Cell       Date:  2022-03-29       Impact factor: 11.277

Review 4.  Role of phasiRNAs in plant-pathogen interactions: molecular perspectives and bioinformatics tools.

Authors:  S Jyothsna; Manickavelu Alagu
Journal:  Physiol Mol Biol Plants       Date:  2022-05-27

5.  Further Elucidation of the Argonaute and Dicer Protein Families in the Model Grass Species Brachypodium distachyon.

Authors:  Ena Šečić; Silvia Zanini; Karl-Heinz Kogel
Journal:  Front Plant Sci       Date:  2019-10-22       Impact factor: 5.753

Review 6.  Tapetum-Dependent Male Meiosis Progression in Plants: Increasing Evidence Emerges.

Authors:  Xiaoning Lei; Bing Liu
Journal:  Front Plant Sci       Date:  2020-01-16       Impact factor: 5.753

7.  Oxygen, secreted proteins and small RNAs: mobile elements that govern anther development.

Authors:  Stefanie Dukowic-Schulze; Karina van der Linde
Journal:  Plant Reprod       Date:  2021-01-25       Impact factor: 3.767

Review 8.  Biogenesis, Functions, Interactions, and Resources of Non-Coding RNAs in Plants.

Authors:  Haoyu Chao; Yueming Hu; Liang Zhao; Saige Xin; Qingyang Ni; Peijing Zhang; Ming Chen
Journal:  Int J Mol Sci       Date:  2022-03-28       Impact factor: 5.923

9.  Reproductive phasiRNA loci and DICER-LIKE5, but not microRNA loci, diversified in monocotyledonous plants.

Authors:  Parth Patel; Sandra M Mathioni; Reza Hammond; Alex E Harkess; Atul Kakrana; Siwaret Arikit; Ayush Dusia; Blake C Meyers
Journal:  Plant Physiol       Date:  2021-04-23       Impact factor: 8.340

10.  Reproductive phasiRNAs regulate reprogramming of gene expression and meiotic progression in rice.

Authors:  Yu-Chan Zhang; Meng-Qi Lei; Yan-Fei Zhou; Yu-Wei Yang; Jian-Ping Lian; Yang Yu; Yan-Zhao Feng; Ke-Reng Zhou; Rui-Rui He; Huang He; Zhi Zhang; Jian-Hua Yang; Yue-Qin Chen
Journal:  Nat Commun       Date:  2020-11-27       Impact factor: 14.919

  10 in total

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