Target Landscape of Conserved Plant MicroRNAs and the Complexities of Their Ancient MicroRNA-Binding Sites

被引:1
|
作者
Wong, Gigi Y. [1 ]
Millar, Anthony A. [1 ]
机构
[1] Australian Natl Univ, Res Sch Biol, Div Plant Sci, Canberra, ACT 2601, Australia
关键词
Land plants; MicroRNA; MicroRNA target; RNA degradome; RNA secondary structure; VARIABLE EFFICACIES; REGULATED GENES; DOWN-REGULATION; ARABIDOPSIS; SEQUENCE; EXPRESSION; RNA; IDENTIFICATION; PREDICTION; MIR159;
D O I
10.1093/pcp/pcad019
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
In plants, microRNA (miRNA)-target interactions (MTIs) require high complementarity, a feature from which bioinformatic programs have predicted numerous and diverse targets for any given miRNA, promoting the idea of complex miRNA networks. Opposing this is a hypothesis of constrained miRNA specificity, in which functional MTIs are restricted to the few targets whose required expression output is compatible with the expression of the miRNA. To explore these opposing views, the bioinformatic pipeline Targets Ranked Using Experimental Evidence was applied to strongly conserved miRNAs to identity their high-evidence (HE) targets across species. For each miRNA family, HE targets predominantly consisted of homologs from one conserved target gene family (primary family). These primary families corresponded to the known canonical miRNA-target families, validating the approach. Very few additional HE target families were identified (secondary family), and if so, they were likely functionally related to the primary family. Many primary target families contained highly conserved nucleotide sequences flanking their miRNA-binding sites that were enriched in HE homologs across species. A number of these flanking sequences are predicted to form conserved RNA secondary structures that preferentially base pair with the miRNA-binding site, implying that these sites are highly structured. Our findings support a target landscape view that is dominated by the conserved primary target families, with a minority of either secondary target families or non-conserved targets. This is consistent with the constrained hypothesis of functional miRNA specificity, which potentially in part is being facilitated by features beyond complementarity.
引用
收藏
页码:604 / 621
页数:18
相关论文
共 50 条
  • [1] Target mRNAs are repressed as efficiently by microRNA-binding sites in the 5′ UTR as in the 3′ UTR
    Lytle, J. Robin
    Yario, Therese A.
    Steitz, Joan A.
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2007, 104 (23) : 9667 - 9672
  • [2] Role of variations within microRNA-binding sites in cancer
    Landi, Debora
    Gemignani, Federica
    Landi, Stefano
    [J]. MUTAGENESIS, 2012, 27 (02) : 205 - 210
  • [3] Single nucleotide variations within and around microRNA-binding sites
    Budmark, Amber
    Catalano, Michael
    Haley, Tyrel
    Hicks, Brady
    Koenen, Maria
    Patrick, Thea
    Larson, Tyler
    Wagner, Tyler
    Butler, Clark
    Feiner, Joshua
    Frick, Rebecca
    Haage, Sierra
    Miller, James
    Nohr, Mackayla
    Stadlman, Dillon
    Turner, Dillon
    Husher, Sara
    Woslum, Nicholas
    Stadem, Nathan
    Dosch, John
    Fortuna, Tyler
    Fredrich, Chandler
    Hadley, Elise
    Oehlerking, Brooklynn
    Paulson, Delayna
    Wiese, Cal
    Mazzer, Paula
    Mullican, Tim
    Anderson, Cynthia
    Larson, Mark
    Paryiskaya, Elena
    Kharazova, Alexandra
    Vermeer, Paola
    Milanovich, Samuel
    Savinov, Alexei
    Collins, John
    Kofman, Alexander
    [J]. CANCER RESEARCH, 2018, 78 (13)
  • [4] Haplotyping of putative microRNA-binding sites in the SNAP-25 gene
    Kovacs-Nagy, Reka
    Sarkozy, Peter
    Hu, Jimmy
    Guttman, Andras
    Sasvari-Szekely, Maria
    Ronai, Zsolt
    [J]. ELECTROPHORESIS, 2011, 32 (15) : 2013 - 2020
  • [5] Human polymorphism at microRNAs and microRNA target sites
    Saunders, Matthew A.
    Liang, Han
    Li, Wen-Hsiung
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2007, 104 (09) : 3300 - 3305
  • [6] On the availability of microRNA-induced silencing complexes, saturation of microRNA-binding sites and stoichiometry
    Mayya, Vinay K.
    Duchaine, Thomas F.
    [J]. NUCLEIC ACIDS RESEARCH, 2015, 43 (15) : 7556 - 7565
  • [7] Association of polymorphisms in microRNA-binding sites and colorectal cancer in an Iranian population
    Azimzadeh, Pedram
    Romani, Sara
    Mohebbi, Seyed Reza
    Mahmoudi, Touraj
    Vahedi, Mohsen
    Fatemi, Seyed Reza
    Zali, Narges
    Zali, Mohammad Reza
    [J]. CANCER GENETICS, 2012, 205 (10) : 501 - 507
  • [8] Screening SNPs residing in the microRNA-binding sites of Hepatocellular Carcinoma related genes
    Ding, Jun
    Gao, Yuzhen
    He, Yan
    Zhou, Yifeng
    Huang, Moli
    Liu, Haiyan
    [J]. INTERNATIONAL JOURNAL OF DATA MINING AND BIOINFORMATICS, 2011, 5 (01) : 1 - 21
  • [9] Evaluation of polymorphisms in microRNA-binding sites and pancreatic cancer risk in Chinese population
    Ke, Juntao
    Peng, Xiating
    Mei, Shufang
    Tian, Jianbo
    Ying, Pingting
    Yang, Nan
    Wang, Xiaoyang
    Zou, Danyi
    Yang, Yang
    Zhu, Ying
    Gong, Yajie
    Gong, Jing
    Zhong, Rong
    Chang, Jiang
    Fang, Zemin
    Miao, Xiaoping
    [J]. JOURNAL OF CELLULAR AND MOLECULAR MEDICINE, 2020, 24 (03) : 2252 - 2259
  • [10] Genetic variants in the integrin gene predicted microRNA-binding sites were associated with the risk of prostate cancer
    Liu, Jiaming
    Huang, Jin
    He, Yazhou
    Liu, Jinnan
    Liao, Banghua
    Liao, Ga
    [J]. MOLECULAR CARCINOGENESIS, 2014, 53 (04) : 280 - 285