Quantitative Proteomics Identify Novel miR-155 Target Proteins

被引:27
|
作者
Loessner, Christopher
Meier, Jan [1 ]
Warnken, Uwe
Rogers, Michael A. [1 ]
Lichter, Peter [1 ]
Pscherer, Armin [1 ]
Schnoelzer, Martina
机构
[1] German Canc Res Ctr, Div Mol Genet, Heidelberg, Germany
来源
PLOS ONE | 2011年 / 6卷 / 07期
关键词
MICRORNA-BINDING-SITES; MESSENGER-RNAS; POSTTRANSCRIPTIONAL REGULATION; AMINO-ACIDS; IDENTIFICATION; INITIATION; TRANSLATION; EXPRESSION; BIOGENESIS; INHIBITION;
D O I
10.1371/journal.pone.0022146
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background: MicroRNAs are 22 nucleotides long non-coding RNAs and exert their function either by transcriptional or translational inhibition. Although many microRNA profiles in different tissues and disease states have already been discovered, only little is known about their target proteins. The microRNA miR-155 is deregulated in many diseases, including cancer, where it might function as an oncoMir. Methodology/Principal Findings: We employed a proteomics technique called "stable isotope labelling by amino acids in cell culture" (SILAC) allowing relative quantification to reliably identify target proteins of miR-155. Using SILAC, we identified 46 putative miR-155 target proteins, some of which were previously reported. With luciferase reporter assays, CKAP5 was confirmed as a new target of miR-155. Functional annotation of miR-155 target proteins pointed to a role in cell cycle regulation. Conclusions/Significance: To the best of our knowledge we have investigated for the first time miR-155 target proteins in the HEK293T cell line in large scale. In addition, by comparing our results to previously identified miR-155 target proteins in other cell lines, we provided further evidence for the cell line specificity of microRNAs.
引用
收藏
页数:11
相关论文
共 50 条
  • [1] miR-155: A Novel Target in Allergic Asthma
    Zhou, Hong
    Li, Junyao
    Gao, Peng
    Wang, Qi
    Zhang, Jie
    INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2016, 17 (10):
  • [2] miR-155 as a novel clinical target for hematological malignancies
    Witten, Lisa
    Slack, Frank J.
    CARCINOGENESIS, 2020, 41 (01) : 2 - 7
  • [3] Inhibition of the miR-155 target NIAM phenocopies the growth promoting effect of miR-155 in B-cell lymphoma
    Slezak-Prochazka, Izabella
    Kluiver, Joost
    de Jong, Debora
    Smigielska-Czepiel, Katarzyna
    Kortman, Gertrud
    Winkle, Melanie
    Rutgers, Bea
    Koerts, Jasper
    Visser, Lydia
    Diepstra, Arjan
    Kroesen, Bart-Jan
    van den Berg, Anke
    ONCOTARGET, 2016, 7 (03) : 2391 - 2400
  • [4] Identification of Novel miR-21 Target Proteins in Multiple Myeloma Cells by Quantitative Proteomics
    Xiong, Qian
    Zhong, Qiu
    Zhang, Jia
    Yang, Mingkun
    Li, Chongyang
    Zheng, Peng
    Bi, Li-Jun
    Ge, Feng
    JOURNAL OF PROTEOME RESEARCH, 2012, 11 (04) : 2078 - 2090
  • [5] Tumor Suppressor PTPRJ Is a Target of miR-155 in Colorectal Cancer
    Zhang, Xiao-Fei
    Tu, Rongfu
    Li, Keke
    Ye, Pengxiang
    Cui, Xiaofeng
    JOURNAL OF CELLULAR BIOCHEMISTRY, 2017, 118 (10) : 3391 - 3400
  • [6] Physiological roles of miR-155
    Mashima, Ryuichi
    IMMUNOLOGY, 2015, 145 (03) : 323 - 333
  • [7] miR-155 in the Resolution of Atherosclerosis
    Bruen, Robyn
    Fitzsimons, Stephen
    Belton, Orina
    FRONTIERS IN PHARMACOLOGY, 2019, 10
  • [8] Inositol phosphatase SHIP1 is a primary target of miR-155
    O'Connell, Ryan M.
    Chaudhuri, Aadel A.
    Rao, Dinesh S.
    Baltimore, David
    PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2009, 106 (17) : 7113 - 7118
  • [9] Hypermethylation of the miR-155 gene in the whole blood and decreased plasma level of miR-155 in rheumatoid arthritis
    Kolarz, Bogdan
    Ciesla, Marek
    Dryglewska, Magdalena
    Rosenthal, Ann K.
    Majdan, Maria
    PLOS ONE, 2020, 15 (06):
  • [10] Roles of the miR-155 in Neuroinflammation and Neurological Disorders: A Potent Biological and Therapeutic Target
    Rastegar-Moghaddam, Seyed Hamidreza
    Ebrahimzadeh-Bideskan, Alireza
    Shahba, Sara
    Malvandi, Amir Mohammad
    Mohammadipour, Abbas
    CELLULAR AND MOLECULAR NEUROBIOLOGY, 2023, 43 (02) : 455 - 467