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The microRNAs in an Ancient Protist Repress the Variant-Specific Surface Protein Expression by Targeting the Entire Coding Sequence


microRNAs (miRNA) have been detected in the deeply branched protist, Giardia lamblia, and shown to repress expression of the family of variant-specific surface proteins (VSPs), only one of which is expressed in Giardia trophozoite at a given time. Three next-generation sequencing libraries of Giardia Argonaute-associated small RNAs were constructed and analyzed. Analysis of the libraries identified a total of 99 new putative miRNAs with a size primarily in the 26 nt range similar to the size previously predicted by the Giardia Dicer crystal structure and identified by our own studies. Bioinformatic analysis identified multiple putative miRNA target sites in the mRNAs of all 73 VSPs. The effect of miRNA target sites within a defined 3′-region were tested on two vsp mRNAs. All the miRNAs showed partial repression of the corresponding vsp expression and were additive when the targeting sites were separately located. But the combined repression still falls short of 100%. Two other relatively short vsp mRNAs with 15 and 11 putative miRNA target sites identified throughout their ORFs were tested with their corresponding miRNAs. The results indicate that; (1) near 100% repression of vsp mRNA expression can be achieved through the combined action of multiple miRNAs on target sites located throughout the ORF; (2) the miRNA machinery could be instrumental in repressing the expression of vsp genes in Giardia; (3) this is the first time that all the miRNA target sites in the entire ORF of a mRNA have been tested and shown to be functional.


Vyšlo v časopise: The microRNAs in an Ancient Protist Repress the Variant-Specific Surface Protein Expression by Targeting the Entire Coding Sequence. PLoS Pathog 10(2): e32767. doi:10.1371/journal.ppat.1003791
Kategorie: Research Article
prolekare.web.journal.doi_sk: https://doi.org/10.1371/journal.ppat.1003791

Souhrn

microRNAs (miRNA) have been detected in the deeply branched protist, Giardia lamblia, and shown to repress expression of the family of variant-specific surface proteins (VSPs), only one of which is expressed in Giardia trophozoite at a given time. Three next-generation sequencing libraries of Giardia Argonaute-associated small RNAs were constructed and analyzed. Analysis of the libraries identified a total of 99 new putative miRNAs with a size primarily in the 26 nt range similar to the size previously predicted by the Giardia Dicer crystal structure and identified by our own studies. Bioinformatic analysis identified multiple putative miRNA target sites in the mRNAs of all 73 VSPs. The effect of miRNA target sites within a defined 3′-region were tested on two vsp mRNAs. All the miRNAs showed partial repression of the corresponding vsp expression and were additive when the targeting sites were separately located. But the combined repression still falls short of 100%. Two other relatively short vsp mRNAs with 15 and 11 putative miRNA target sites identified throughout their ORFs were tested with their corresponding miRNAs. The results indicate that; (1) near 100% repression of vsp mRNA expression can be achieved through the combined action of multiple miRNAs on target sites located throughout the ORF; (2) the miRNA machinery could be instrumental in repressing the expression of vsp genes in Giardia; (3) this is the first time that all the miRNA target sites in the entire ORF of a mRNA have been tested and shown to be functional.


Zdroje

1. BarwickRS, LevyDA, CraunGF, BeachMJ, CalderonRL (2000) Surveillance for waterborne-disease outbreaks–United States, 1997–1998. MMWR CDC Surveill Summ 49: 1–21.

2. SavioliL, SmithH, ThompsonA (2006) Giardia and Cryptosporidium join the ‘Neglected Diseases Initiative’. Trends Parasitol 22: 203–208.

3. AdamRD, NigamA, SeshadriV, MartensCA, FarnethGA, et al. (2010) The Giardia lamblia vsp gene repertoire: characteristics, genomic organization, and evolution. BMC Genomics 11: 424.

4. NashTE, BanksSM, AllingDW, MerrittJWJr, ConradJT (1990) Frequency of variant antigens in Giardia lamblia. Exp Parasitol 71: 415–421.

5. NashTE, LujanHT, MowattMR, ConradJT (2001) Variant-specific surface protein switching in Giardia lamblia. Infect Immun 69: 1922–1923.

6. DeitschKW, LukehartSA, StringerJR (2009) Common strategies for antigenic variation by bacterial, fungal and protozoan pathogens. Nat Rev Microbiol 7: 493–503.

7. LiW, SaraiyaAA, WangCC (2013) Experimental Verification of the Identity of Variant-Specific Surface Proteins in Giardia lamblia Trophozoites. MBio 4: e00321–13.

8. MowattMR, AggarwalA, NashTE (1991) Carboxy-terminal sequence conservation among variant-specific surface proteins of Giardia lamblia. Mol Biochem Parasitol 49: 215–227.

9. NashTE, MowattMR (1992) Characterization of a Giardia lamblia variant-specific surface protein (VSP) gene from isolate GS/M and estimation of the VSP gene repertoire size. Mol Biochem Parasitol 51: 219–227.

10. PruccaCG, SlavinI, QuirogaR, EliasEV, RiveroFD, et al. (2008) Antigenic variation in Giardia lamblia is regulated by RNA interference. Nature 456: 750–754.

11. FaghiriZ, WidmerG (2011) A comparison of the Giardia lamblia trophozoite and cyst transcriptome using microarrays. BMC Microbiol 11: 91.

12. LiW, SaraiyaAA, WangCC (2011) Gene regulation in Giardia lambia involves a putative microRNA derived from a small nucleolar RNA. PLoS Negl Trop Dis 5: e1338.

13. LiW, SaraiyaAA, WangCC (2012) The profile of snoRNA-derived microRNAs that regulate expression of variant surface proteins in Giardia lamblia. Cell Microbiol 14: 1455–73.

14. SaraiyaAA, LiW, WangCC (2011) A microRNA derived from an apparent canonical biogenesis pathway regulates variant surface protein gene expression in Giardia lamblia. RNA 17: 2152–2164.

15. SaraiyaAA, LiW, WangCC (2013) Transition of a microRNA from repressing to activating translation depending on the extent of base pairing with the target. PLoS One 8: e55672.

16. SaraiyaAA, WangCC (2008) snoRNA, a novel precursor of microRNA in Giardia lamblia. PLoS Pathog 4: e1000224.

17. KrolJ, LoedigeI, FilipowiczW (2010) The widespread regulation of microRNA biogenesis, function and decay. Nat Rev Genet 11: 597–610.

18. BazziniAA, LeeMT, GiraldezAJ (2012) Ribosome profiling shows that miR-430 reduces translation before causing mRNA decay in zebrafish. Science 336: 233–237.

19. DjuranovicS, NahviA, GreenR (2012) miRNA-mediated gene silencing by translational repression followed by mRNA deadenylation and decay. Science 336: 237–240.

20. BartelDP (2009) MicroRNAs: target recognition and regulatory functions. Cell 136: 215–233.

21. PasquinelliAE (2012) MicroRNAs and their targets: recognition, regulation and an emerging reciprocal relationship. Nat Rev Genet 13: 271–282.

22. DuursmaAM, KeddeM, SchrierM, le SageC, AgamiR (2008) miR-148 targets human DNMT3b protein coding region. RNA 14: 872–877.

23. ElchevaI, GoswamiS, NoubissiFK, SpiegelmanVS (2009) CRD-BP protects the coding region of betaTrCP1 mRNA from miR-183-mediated degradation. Mol Cell 35: 240–246.

24. MandkeP, WyattN, FraserJ, BatesB, BerberichSJ, et al. (2012) MicroRNA-34a modulates MDM4 expression via a target site in the open reading frame. PLoS One 7: e42034.

25. ShenWF, HuYL, UttarwarL, PassegueE, LargmanC (2008) MicroRNA-126 regulates HOXA9 by binding to the homeobox. Mol Cell Biol 28: 4609–4619.

26. TayYM, TamWL, AngYS, GaughwinPM, YangH, et al. (2008) MicroRNA-134 modulates the differentiation of mouse embryonic stem cells, where it causes post-transcriptional attenuation of Nanog and LRH1. Stem Cells 26: 17–29.

27. YiC, XieWD, LiF, LvQ, HeJ, et al. (2011) MiR-143 enhances adipogenic differentiation of 3T3-L1 cells through targeting the coding region of mouse pleiotrophin. FEBS Lett 585: 3303–3309.

28. JungHM, PatelRS, PhillipsBL, WangH, CohenDM, et al. (2013) Tumor suppressor miR-375 regulates MYC expression via repression of CIP2A coding sequence through multiple miRNA-mRNA interactions. Mol Biol Cell 24: 1638–1637, 1638-1648, S1631-1637.

29. QinW, ShiY, ZhaoB, YaoC, JinL, et al. (2010) miR-24 regulates apoptosis by targeting the open reading frame (ORF) region of FAF1 in cancer cells. PLoS One 5: e9429.

30. FormanJJ, Legesse-MillerA, CollerHA (2008) A search for conserved sequences in coding regions reveals that the let-7 microRNA targets Dicer within its coding sequence. Proc Natl Acad Sci U S A 105: 14879–14884.

31. GuS, JinL, ZhangF, SarnowP, KayMA (2009) Biological basis for restriction of microRNA targets to the 3′ untranslated region in mammalian mRNAs. Nat Struct Mol Biol 16: 144–150.

32. ChiSW, ZangJB, MeleA, DarnellRB (2009) Argonaute HITS-CLIP decodes microRNA-mRNA interaction maps. Nature 460: 479–486.

33. ZisoulisDG, LovciMT, WilbertML, HuttKR, LiangTY, et al. (2010) Comprehensive discovery of endogenous Argonaute binding sites in Caenorhabditis elegans. Nat Struct Mol Biol 17: 173–179.

34. FangZ, RajewskyN (2011) The impact of miRNA target sites in coding sequences and in 3′UTRs. PLoS One 6: e18067.

35. AdamRD (2000) The Giardia lamblia genome. Int J Parasitol 30: 475–484.

36. AdamRD (2001) Biology of Giardia lamblia. Clin Microbiol Rev 14: 447–475.

37. FranzenO, Jerlstrom-HultqvistJ, EinarssonE, AnkarklevJ, FerellaM, et al. (2013) Transcriptome profiling of Giardia intestinalis using strand-specific RNA-seq. PLoS Comput Biol 9: e1003000.

38. LangmeadB, TrapnellC, PopM, SalzbergSL (2009) Ultrafast and memory-efficient alignment of short DNA sequences to the human genome. Genome Biol 10: R25.

39. AurrecoecheaC, BrestelliJ, BrunkBP, CarltonJM, DommerJ, et al. (2009) GiardiaDB and TrichDB: integrated genomic resources for the eukaryotic protist pathogens Giardia lamblia and Trichomonas vaginalis. Nucleic Acids Res 37: D526–530.

40. MacraeIJ, ZhouK, LiF, RepicA, BrooksAN, et al. (2006) Structural basis for double-stranded RNA processing by Dicer. Science 311: 195–198.

41. HofackerIL, FontanaW, StadlerPF, BonhoefferLS, TackerM, et al. (1994) Fast folding and comparison of RNA secondary structures. Monatshefte für Chemie/Chemical Monthly 125: 167–188.

42. HofackerIL, StadlerPF (2006) Memory efficient folding algorithms for circular RNA secondary structures. Bioinformatics 22: 1172–1176.

43. MacRaeIJ, ZhouK, DoudnaJA (2007) Structural determinants of RNA recognition and cleavage by Dicer. Nat Struct Mol Biol 14: 934–940.

44. ParkJE, HeoI, TianY, SimanshuDK, ChangH, et al. (2011) Dicer recognizes the 5′ end of RNA for efficient and accurate processing. Nature 475: 201–205.

45. EyPL, MansouriM, KuldaJ, NohynkovaE, MonisPT, et al. (1997) Genetic analysis of Giardia from hoofed farm animals reveals artiodactyl-specific and potentially zoonotic genotypes. J Eukaryot Microbiol 44: 626–635.

46. Jerlstrom-HultqvistJ, FranzenO, AnkarklevJ, XuF, NohynkovaE, et al. (2010) Genome analysis and comparative genomics of a Giardia intestinalis assemblage E isolate. BMC Genomics 11: 543.

47. JohnB, EnrightAJ, AravinA, TuschlT, SanderC, et al. (2004) Human MicroRNA targets. PLoS Biol 2: e363.

48. LiL, WangCC (2004) Capped mRNA with a single nucleotide leader is optimally translated in a primitive eukaryote, Giardia lamblia. J Biol Chem 279: 14656–14664.

49. KeisterDB (1983) Axenic culture of Giardia lamblia in TYI-S-33 medium supplemented with bile. Trans R Soc Trop Med Hyg 77: 487–488.

Štítky
Hygiena a epidemiológia Infekčné lekárstvo Laboratórium

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PLOS Pathogens


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