Cited by 155

Target-Mediated Protection of Endogenous MicroRNAs in C. elegans

Chatterjee, Saibal, Fasler, Monika, Büssing, Ingo, Großhans, Helge·2011·Developmental Cell

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Integrity signals

Registry

Crossref · 10.1016/j.devcel.2011.02.008

Cites

1 of 1 references verified0 citation errors · 0 not checkable

Statistics

Claims the paper makes

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

  • Depletion or reduction of the 5'->3' exonucleases xrn-1 and xrn-2 result in accumulation of specific miRNAs and miR* strands.

    “Further, depletion or reduction of the 5′ ➔ 3′ exonucleases xrn‐1 and xrn‐2 result in accumulation of specific miRNAs and miR* strands (Chatterjee et al., 2011).”

    From microRNA strand selection: Unwinding the rules (2021) · cites this paper as Chatterjee et al., 2011

  • Reduction of xrn-1 or xrn-2 affects the 5p/3p ratios of certain miRNAs.

    “Interestingly, this effect is not equal—reduction of xrn‐1 or xrn‐2 have been shown to affect the 5p/3p ratios of certain miRNAs (Chatterjee et al., 2011; Miki, Rüegger, Gaidatzis, Stadler, & Großhans, 2014).”

    From microRNA strand selection: Unwinding the rules (2021) · cites this paper as Chatterjee et al., 2011

  • The ratio of miR::miR* strands may be influenced by target availability, as the presence of suitable mRNA targets can stabilize cognate miRNAs.

    “It has been suggested that the ratio of miR::miR* strands may be influenced by target availability, as the presence of suitable mRNA targets can stabilize cognate miRNAs (Chatterjee, Fasler, Büssing, & Großhans, 2011; Tsai et al., 2016).”

    From microRNA strand selection: Unwinding the rules (2021) · cites this paper as Chatterjee, Fasler, Büssing, & Großhans, 2011

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

Cites

Flagged first, then by citations

Research works printed but not linked: 36

  1. [1]1. Ameres, S.L. ∙ Horwich, M.D. ∙ Hung, J.H. ... Target RNA-directed trimming and tailing of small silencing RNAs Science. 2010; 328:1534-1539 Crossref Scopus (459) PubMed Google Scholar
  2. [2]2. Bail, S. ∙ Swerdel, M. ∙ Liu, H. ... Differential regulation of microRNA stability RNA. 2010; 16:1032-1039 Crossref Scopus (239) PubMed Google Scholar
  3. [3]3. Bushati, N. ∙ Cohen, S.M. microRNA functions Annu. Rev. Cell Dev. Biol. 2007; 23:175-205 Crossref Scopus (2555) PubMed Google Scholar
  4. [4]4. Büssing, I. ∙ Yang, J.S. ∙ Lai, E.C. ... The nuclear export receptor XPO-1 supports primary miRNA processing in C. elegans and Drosophila EMBO J. 2010; 29:1830-1839 Crossref Scopus (62) PubMed Google Scholar
  5. [5]5. Carthew, R.W. ∙ Sontheimer, E.J. Origins and mechanisms of miRNAs and siRNAs Cell. 2009; 136:642-655 Full Text Full Text (PDF) Scopus (4123) PubMed Google Scholar
  6. [6]6. Cazalla, D. ∙ Yario, T. ∙ Steitz, J. Down-regulation of a host microRNA by a Herpesvirus saimiri noncoding RNA Science. 2010; 328:1563-1566 Crossref Scopus (403) PubMed Google Scholar
  7. [7]7. Chatterjee, S. ∙ Großhans, H. Active turnover modulates mature microRNA activity in Caenorhabditis elegans Nature. 2009; 461:546-549 Crossref Scopus (295) PubMed Google Scholar
  8. [8]8. Chiang, H.R. ∙ Schoenfeld, L.W. ∙ Ruby, J.G. ... Mammalian microRNAs: experimental evaluation of novel and previously annotated genes Genes Dev. 2010; 24:992-1009 Crossref Scopus (681) PubMed Google Scholar
  9. [9]9. Czech, B. ∙ Zhou, R. ∙ Erlich, Y. ... Hierarchical rules for Argonaute loading in Drosophila Mol. Cell. 2009; 36:445-456 Full Text Full Text (PDF) Scopus (217) PubMed Google Scholar
  10. [10]10. de Wit, E. ∙ Linsen, S.E. ∙ Cuppen, E. ... Repertoire and evolution of miRNA genes in four divergent nematode species Genome Res. 2009; 19:2064-2074 Crossref Scopus (100) PubMed Google Scholar
  11. [11]11. Ding, X.C. ∙ Slack, F.J. ∙ Großhans, H. The let-7 microRNA interfaces extensively with the translation machinery to regulate cell differentiation Cell Cycle. 2008; 7:3083-3090 Crossref Scopus (42) PubMed Google Scholar
  12. [12]12. Ghildiyal, M. ∙ Xu, J. ∙ Seitz, H. ... Sorting of Drosophila small silencing RNAs partitions microRNA∗ strands into the RNA interference pathway RNA. 2010; 16:43-56 Crossref Scopus (293) PubMed Google Scholar
  13. [13]13. Griffiths-Jones, S. ∙ Saini, H.K. ∙ Dongen, S.V. ... miRBase: tools for microRNA genomics Nucleic Acids Res. 2007; 36:D154-D158 Crossref Scopus (3769) PubMed Google Scholar
  14. [14]14. Großhans, H. ∙ Johnson, T. ∙ Reinert, K.L. ... The temporal patterning microRNA let-7 regulates several transcription factors at the larval to adult transition in C. elegans Dev. Cell. 2005; 8:321-330 Full Text Full Text (PDF) Scopus (216) PubMed Google Scholar
  15. [15]15. Han, J. ∙ Lee, Y. ∙ Yeom, K.H. ... Molecular basis for the recognition of primary microRNAs by the Drosha-DGCR8 complex Cell. 2006; 125:887-901 Full Text Full Text (PDF) Scopus (1220) PubMed Google Scholar
  16. [16]16. Hayes, G.D. ∙ Frand, A.R. ∙ Ruvkun, G. The mir-84 and let-7 paralogous microRNA genes of Caenorhabditis elegans direct the cessation of molting via the conserved nuclear hormone receptors NHR-23 and NHR-25 Development. 2006; 133:4631-4641 Crossref Scopus (84) PubMed Google Scholar
  17. [17]17. Henry, Y. ∙ Wood, H. ∙ Morrissey, J.P. ... The 5′ end of yeast 5.8S rRNA is generated by exonucleases from an upstream cleavage site EMBO J. 1994; 13:2452-2463 Crossref Scopus (272) PubMed Google Scholar
  18. [18]18. Hurschler, B.A. ∙ Harris, D.T. ∙ Großhans, H. The type II poly(A)-binding protein PABP-2 genetically interacts with the let-7 miRNA and elicits heterochronic phenotypes in C. elegans Nucl. Acids Res. 2011; in press Crossref Scopus (15) Google Scholar
  19. [19]19. Hutvagner, G. ∙ Simard, M.J. ∙ Mello, C.C. ... Sequence-specific inhibition of small RNA function PLoS Biol. 2004; 2:E98 Crossref Scopus (583) PubMed Google Scholar
  20. [20]20. Kamath, R.S. ∙ Fraser, A.G. ∙ Dong, Y. ... Systematic functional analysis of the Caenorhabditis elegans genome using RNAi Nature. 2003; 421:231-237 Crossref Scopus (2877) PubMed Google Scholar
  21. [21]21. Kato, M. ∙ de Lencastre, A. ∙ Pincus, Z. ... Dynamic expression of small non-coding RNAs, including novel microRNAs and piRNAs/21U-RNAs, during Caenorhabditis elegans development Genome Biol. 2009; 10:R54 Crossref Scopus (121) PubMed Google Scholar
  22. [22]22. Khvorova, A. ∙ Reynolds, A. ∙ Jayasena, S.D. Functional siRNAs and miRNAs exhibit strand bias Cell. 2003; 115:209-216 Full Text Full Text (PDF) Scopus (2095) PubMed Google Scholar
  23. [23]23. Krüger, J. ∙ Rehmsmeier, M. RNAhybrid: microRNA target prediction easy, fast and flexible Nucleic Acids Res. 2006; 34:W451-W454 Crossref Scopus (1432) PubMed Google Scholar
  24. [24]24. Moss, E.G. ∙ Lee, R.C. ∙ Ambros, V. The cold shock domain protein LIN-28 controls developmental timing in C. elegans and is regulated by the lin-4 RNA Cell. 1997; 88:637-646 Full Text Full Text (PDF) Scopus (713) PubMed Google Scholar
  25. [25]25. Okamura, K. ∙ Liu, N. ∙ Lai, E.C. Distinct mechanisms for microRNA strand selection by Drosophila Argonautes Mol. Cell. 2009; 36:431-444 Full Text Full Text (PDF) Scopus (243) PubMed Google Scholar
  26. [26]26. Okamura, K. ∙ Phillips, M.D. ∙ Tyler, D.M. ... The regulatory activity of microRNA(∗) species has substantial influence on microRNA and 3′ UTR evolution Nat. Struct. Mol. Biol. 2008; 15:354-363 Crossref Scopus (445) PubMed Google Scholar
  27. [27]27. Petfalski, E. ∙ Dandekar, T. ∙ Henry, Y. ... Processing of the precursors to small nucleolar RNAs and rRNAs requires common components Mol. Cell. Biol. 1998; 18:1181-1189 Crossref Scopus (181) PubMed Google Scholar
  28. [28]28. Pillai, R.S. ∙ Bhattacharyya, S.N. ∙ Artus, C.G. ... Inhibition of translational initiation by Let-7 microRNA in human cells Science. 2005; 309:1573-1576 Crossref Scopus (1158) PubMed Google Scholar
  29. [29]29. Poole, T.L. ∙ Stevens, A. Comparison of features of the RNase activity of 5′-exonuclease-1 and 5′-exonuclease-2 of Saccharomyces cerevisiae Nucleic Acids Symp. Ser. 1995; 33:79-81 PubMed Google Scholar
  30. [30]30. Reinhart, B.J. ∙ Slack, F.J. ∙ Basson, M. ... The 21-nucleotide let-7 RNA regulates developmental timing in Caenorhabditis elegans Nature. 2000; 403:901-906 Crossref Scopus (3972) PubMed Google Scholar
  31. [31]31. Resnick, T.D. ∙ McCulloch, K.A. ∙ Rougvie, A.E. miRNAs give worms the time of their lives: small RNAs and temporal control in Caenorhabditis elegans Dev. Dyn. 2010; 239:1477-1489 PubMed Google Scholar
  32. [32]32. Ruby, J.G. ∙ Jan, C. ∙ Player, C. ... Large-scale sequencing reveals 21U-RNAs and additional microRNAs and endogenous siRNAs in C. elegans Cell. 2006; 127:1193-1207 Full Text Full Text (PDF) Scopus (773) PubMed Google Scholar
  33. [33]33. Schwarz, D.S. ∙ Hutvágner, G. ∙ Du, T. ... Asymmetry in the assembly of the RNAi enzyme complex Cell. 2003; 115:199-208 Full Text Full Text (PDF) Scopus (2278) PubMed Google Scholar
  34. [34]34. Seitz, H. Redefining MicroRNA Targets Curr. Biol. 2009; 19:870-873 Full Text Full Text (PDF) Scopus (306) PubMed Google Scholar
  35. [35]35. Tomari, Y. ∙ Matranga, C. ∙ Haley, B. ... A protein sensor for siRNA asymmetry Science. 2004; 306:1377-1380 Crossref Scopus (485) PubMed Google Scholar
  36. [36]36. Weidhaas, J.B. ∙ Babar, I. ∙ Nallur, S.M. ... MicroRNAs as potential agents to alter resistance to cytotoxic anticancer therapy Cancer Res. 2007; 67:11111-11116 Crossref Scopus (361) PubMed Google Scholar

Cited by

Sorted by citations

Authors
Chatterjee, S., Fasler, M., Büssing, I., & Großhans, H.
Venue
Developmental Cell
Publisher
Elsevier BV
Published
2011-03
Volume
20
Issue
3
Pages
388-396
ISSN
1534-5807
Cited by
155
References
1
Language
en
Funders
  • European Research Council (ERC 2419845)
  • Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung (31003A_127052)
  • Free Market Institute, Texas Tech University
  • EMBO
  • Marie Curie

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review