Login to MyKarger

New to MyKarger? Click here to sign up.



Login with Facebook

Forgot your password?

Authors, Editors, Reviewers

For Manuscript Submission, Check or Review Login please go to Submission Websites List.

Submission Websites List

Institutional Login
(Shibboleth or OpenAthens)

For the academic login, please select your organization on the next page. You will be redirected to verify your credentials.

OpenAthens/Shibboleth

Regulatory Mechanisms

Small non-coding RNAs and genomic imprinting

Royo H.a · Bortolin M.-L.a · Seitz H.b · Cavaillé J.a

Author affiliations

aLBME-CNRS, UMR 5099, IFR 109, Toulouse (France); bUMMS, Department of Biochemistry and Molecular Pharmacology, Lazare Research Building, Worcester, MA (USA)

Related Articles for ""

Cytogenet Genome Res 113:99–108 (2006)

Do you have an account?

Login Information





Contact Information











I have read the Karger Terms and Conditions and agree.



Login Information





Contact Information











I have read the Karger Terms and Conditions and agree.



To view the fulltext, please log in

To view the pdf, please log in

Buy

  • FullText & PDF
  • Unlimited re-access via MyKarger
  • Unrestricted printing, no saving restrictions for personal use
read more

CHF 38.00 *
EUR 35.00 *
USD 39.00 *

Select

KAB

Buy a Karger Article Bundle (KAB) and profit from a discount!

If you would like to redeem your KAB credit, please log in.


Save over 20% compared to the individual article price.
Learn more

Rent/Cloud

  • Rent for 48h to view
  • Buy Cloud Access for unlimited viewing via different devices
  • Synchronizing in the ReadCube Cloud
  • Printing and saving restrictions apply

Rental: USD 8.50
Cloud: USD 20.00


Select

Subscribe

  • Access to all articles of the subscribed year(s) guaranteed for 5 years
  • Unlimited re-access via Subscriber Login or MyKarger
  • Unrestricted printing, no saving restrictions for personal use
read more

Subcription rates


Select

* The final prices may differ from the prices shown due to specifics of VAT rules.

Article / Publication Details

First-Page Preview
Abstract of Regulatory Mechanisms

Published online: March 30, 2006
Issue release date: March 2006

Number of Print Pages: 10
Number of Figures: 3
Number of Tables: 0

ISSN: 1424-8581 (Print)
eISSN: 1424-859X (Online)

For additional information: https://www.karger.com/CGR

Abstract

Experimental and computer-assisted approaches have led to the identification of hundreds of imprinted small RNA genes, mainly clustered in two chromosomal domains (human 15q11→q13 and 14q32 loci). The genes are only detected in placental mammals and belong to the C/D RNA and microRNA gene families. These are small non-coding RNAs involved in RNA-guided post-transcriptional RNA modifications and RNA-mediated gene silencing, respectively. Here, we discuss their potential functions and report the identification of novel small RNA genes lying within (or nearby) known imprinted chromosomal domains.

© 2006 S. Karger AG, Basel




Related Articles:


References

  1. Almeida R, Allshire RC: RNA silencing and genome regulation. Trends Cell Biol 15:251–258 (2005).
  2. Altuvia Y, Landgraf P, Lithwick G, Elefant N, Pfeffer S, Aravin A, et al: Clustering and conservation patterns of human microRNAs. Nucleic Acids Res 33:2697–2706 (2005).
  3. Ambros V: The functions of animal microRNAs. Nature 431:350–355 (2004).
  4. Aukerman MJ, Sakai H: Regulation of flowering time and floral organ identity by a MicroRNA and its APETALA2-like target genes. Plant Cell 15:2730–2741 (2003).
  5. Bachellerie JP, Cavaille J, Huttenhofer A: The expanding snoRNA world. Biochimie 84:775–790 (2002).
  6. Bao N, Lye KW, Barton MK: MicroRNA binding sites in Arabidopsis class III HD-ZIP mRNAs are required for methylation of the template chromosome. Dev Cell 7:653–662 (2004).
  7. Bartel DP: MicroRNAs: genomics, biogenesis, mechanism, and function. Cell 116:281–297 (2004).
  8. Bartel DP, Chen CZ: Micromanagers of gene expression: the potentially widespread influence of metazoan microRNAs. Nat Rev Genet 5:396–400 (2004).
  9. Bentwich I, Avniel A, Karov Y, Aharonov R, Gilad S, Barad O, et al: Identification of hundreds of conserved and nonconserved human microRNAs. Nat Genet 37:766–770 (2005).
  10. Berezikov E, Guryev V, van de Belt J, Wienholds E, Plasterk RH, Cuppen E: Phylogenetic shadowing and computational identification of human microRNA genes. Cell 120:21–24 (2005).
  11. Burns CM, Chu H, Rueter SM, Hutchinson LK, Canton H, Sanders-Bush E, Emeson RB: Regulation of serotonin-2C receptor G-protein coupling by RNA editing. Nature 387:303–308 (1997).
  12. Cavaille J, Buiting K, Kiefmann M, Lalande M, Brannan CI, Horsthemke B, et al: Identification of brain-specific and imprinted small nucleolar RNA genes exhibiting an unusual genomic organization. Proc Natl Acad Sci USA 97:14311–14316 (2000).
  13. Cavaille J, Vitali P, Basyuk E, Huttenhofer A, Bachellerie JP: A novel brain-specific box C/D small nucleolar RNA processed from tandemly repeated introns of a noncoding RNA gene in rats. J Biol Chem 276:26374–26383 (2001).
  14. Cavaille J, Seitz H, Paulsen M, Ferguson-Smith AC, Bachellerie JP: Identification of tandemly-repeated C/D snoRNA genes at the imprinted human 14q32 domain reminiscent of those at the Prader-Willi/Angelman syndrome region. Hum Mol Genet 11:1527–1538 (2002).
  15. Chai JH, Locke DP, Ohta T, Greally JM, Nicholls RD: Retrotransposed genes such as Frat3 in the mouse Chromosome 7C Prader-Willi syndrome region acquire the imprinted status of their insertion site. Mamm Genome 12:813–821 (2001).
  16. Charlier C, Segers K, Karim L, Shay T, Gyapay G, Cockett N, Georges M: The callipyge mutation enhances the expression of coregulated imprinted genes in cis without affecting their imprinting status. Nat Genet 27:367–369 (2001).
  17. Cheng LC, Tavazoie M, Doetsch F: Stem cells: from epigenetics to microRNAs. Neuron 46:363–367 (2005).
  18. Davis E, Jensen CH, Schroder HD, Farnir F, Shay-Hadfield T, Kliem A, et al: Ectopic expression of DLK1 protein in skeletal muscle of padumnal heterozygotes causes the callipyge phenotype. Curr Biol 14:1858–1862 (2004).
  19. Davis E, Caiment F, Tordoir X, Cavaille J, Ferguson-Smith A, Cockett N, Georges M, Charlier C: RNAi-mediated allelic trans-interaction at the imprinted Rtl1/Peg11 locus. Curr Biol 15:743–749 (2005).
  20. de los Santos T, Schweizer J, Rees CA, Francke U: Small evolutionarily conserved RNA, resembling C/D box small nucleolar RNA, is transcribed from PWCR1, a novel imprinted gene in the Prader-Willi deletion region, which is highly expressed in brain. Am J Hum Genet 67:1067–1082 (2000).
  21. Doench JG, Sharp PA: Specificity of microRNA target selection in translational repression. Genes Dev 18:504–511 (2004).
  22. Freking BA, Murphy SK, Wylie AA, Rhodes SJ, Keele JW, Leymaster KA, Jirtle RL, Smith TP: Identification of the single base change causing the callipyge muscle hypertrophy phenotype, the only known example of polar overdominance in mammals. Genome Res 12:1496–1506 (2002).
  23. Fukagawa T, Nogami M, Yoshikawa M, Ikeno M, Okazaki T, Takami Y, Nakayama T, Oshimura M: Dicer is essential for formation of the heterochromatin structure in vertebrate cells. Nat Cell Biol 6:784–791 (2004).
  24. Gallagher RC, Pils B, Albalwi M, Francke U: Evidence for the role of PWCR1/HBII-85 C/D box small nucleolar RNAs in Prader-Willi syndrome. Am J Hum Genet 71:669–678 (2002).
  25. Georges M, Charlier C, Cockett N: The callipyge locus: evidence for the trans interaction of reciprocally imprinted genes. Trends Genet 19:248–252 (2003).
  26. Georgiades P, Watkins M, Surani MA, Ferguson-Smith AC: Parental origin-specific developmental defects in mice with uniparental disomy for chromosome 12. Development 127:4719–4728 (2000).
  27. Giraldez AJ, Cinalli RM, Glasner ME, Enright AJ, Thomson JM, Baskerville S, et al: MicroRNAs regulate brain morphogenesis in zebrafish. Science 308:833–838 (2005).
  28. Heard E: Recent advances in X-chromosome inactivation. Curr Opin Cell Biol 16:247–255 (2004).
  29. Huttenhofer A, Kiefmann M, Meier-Ewert S, O’Brien J, Lehrach H, Bachellerie JP, Brosius J: RNomics: an experimental approach that identifies 201 candidates for novel, small, non-messenger RNAs in mouse. EMBO J 20:2943–2953 (2001).
  30. Huttenhofer A, Schattner P, Polacek N: Non-coding RNAs: hope or hype? Trends Genet 21:289–297 (2005).
  31. Jing Q, Huang S, Guth S, Zarubin T, Motoyama A, Chen J, et al: Involvement of microRNA in AU-rich element-mediated mRNA instability. Cell 120:623–634 (2005).
  32. John B, Enright AJ, Aravin A, Tuschl T, Sander C, Marks DS: Human MicroRNA targets. PLoS Biol 2:e363 (2004).
  33. Kanellopoulou C, Muljo SA, Kung AL, Ganesan S, Drapkin R, Jenuwein T, Livingston DM, Rajewsky K: Dicer-deficient mouse embryonic stem cells are defective in differentiation and centromeric silencing. Genes Dev 19:489–501 (2005).
  34. Kawasaki H, Taira K: Induction of DNA methylation and gene silencing by short interfering RNAs in human cells. Nature 431:211–217 (2004).
  35. Kim J, Krichevsky A, Grad Y, Hayes GD, Kosik KS, Church GM, Ruvkun G: Identification of many microRNAs that copurify with polyribosomes in mammalian neurons. Proc Natl Acad Sci USA 101:360–365 (2004).
  36. Kim VN: MicroRNA biogenesis: coordinated cropping and dicing. Nat Rev Mol Cell Biol 6:376–385 (2005).
  37. Kiriakidou M, Nelson PT, Kouranov A, Fitziev P, Bouyioukos C, Mourelatos Z, Hatzigeorgiou A: A combined computational-experimental approach predicts human microRNA targets. Genes Dev 18:1165–1178 (2004).
  38. Kiss T: Small nucleolar RNAs: an abundant group of noncoding RNAs with diverse cellular functions. Cell 109:145–148 (2002).
  39. Komine Y, Tanaka NK, Yano R, Takai S, Yuasa S, Shiroishi T, Tsuchiya K, Yamamori T: A novel type of non-coding RNA expressed in the rat brain. Brain Res Mol Brain Res 66:1–13 (1999).
  40. Krek A, Grun D, Poy MN, Wolf R, Rosenberg L, Epstein EJ, et al: Combinatorial microRNA target predictions. Nat Genet 37:495–500 (2005).
  41. Landers M, Bancescu DL, Le Meur E, Rougeulle C, Glatt-Deeley H, Brannan C, Muscatelli F, Lalande M: Regulation of the large (approximately 1000 kb) imprinted murine Ube3a antisense transcript by alternative exons upstream of Snurf/Snrpn. Nucleic Acids Res 32:3480–3492 (2004).
  42. Lecellier CH, Dunoyer P, Arar K, Lehmann-Che J, Eyquem S, Himber C, Saib A, Voinnet O: A cellular microRNA mediates antiviral defense in human cells. Science 308:557–560 (2005).
  43. Lefebvre L, Viville S, Barton SC, Ishino F, Keverne EB, Surani MA: Abnormal maternal behaviour and growth retardation associated with loss of the imprinted gene Mest. Nat Genet 20:163–169 (1998).
  44. Lewis BP, Burge CB, Bartel DP: Conserved seed pairing, often flanked by adenosines, indicates that thousands of human genes are microRNA targets. Cell 120:15–20 (2005).
  45. Lim LP, Lau NC, Garrett-Engele P, Grimson A, Schelter JM, Castle J, et al: Microarray analysis shows that some microRNAs downregulate large numbers of target mRNAs. Nature 433:769–773 (2005).
  46. Lin SP, Youngson N, Takada S, Seitz H, Reik W, Paulsen M, Cavaille J, Ferguson-Smith AC: Asymmetric regulation of imprinting on the maternal and paternal chromosomes at the Dlk1-Gtl2 imprinted cluster on mouse chromosome 12. Nat Genet 35:97–102 (2003).
  47. Lynch C, Tristem M: A co-opted gypsy-type LTR-retrotransposon is conserved in the genomes of humans, sheep, mice, and rats. Curr Biol 13:1518–1523 (2003).
  48. Matzke MA, Birchler JA: RNAi-mediated pathways in the nucleus. Nat Rev Genet 6:24–35 (2005).
  49. Meguro M, Mitsuya K, Nomura N, Kohda M, Kashiwagi A, Nishigaki R, et al: Large-scale evaluation of imprinting status in the Prader-Willi syndrome region: an imprinted direct repeat cluster resembling small nucleolar RNA genes. Hum Mol Genet 10:383–394 (2001).
  50. Moore T, Haig D: Genomic imprinting in mammalian development: a parental tug-of-war. Trends Genet 7:45–49 (1991).
  51. Morris KV, Chan SW, Jacobsen SE, Looney DJ: Small interfering RNA-induced transcriptional gene silencing in human cells. Science 305:1289–1292 (2004).
  52. Nicholls RD, Knepper JL: Genome organization, function, and imprinting in Prader-Willi and Angelman syndromes. Annu Rev Genomics Hum Genet 2:153–175 (2001).
  53. Niswender CM, Copeland SC, Herrick-Davis K, Emeson RB, Sanders-Bush E: RNA editing of the human serotonin 5-hydroxytryptamine 2C receptor silences constitutive activity. J Biol Chem 274:9472–9478 (1999).
  54. O’Neill MJ: The influence of non-coding RNAs on allele-specific gene expression in mammals. Hum Mol Genet 14 Spec No 1:R113–120 (2005).
  55. Park CW, Chen Z, Kren BT, Steer CJ: Double-stranded siRNA targeted to the huntingtin gene does not induce DNA methylation. Biochem Biophys Res Commun 323:275–280 (2004).
  56. Plagge A, Isles AR, Gordon E, Humby T, Dean W, Gritsch S, et al: Imprinted Nesp55 influences behavioral reactivity to novel environments. Mol Cell Biol 25:3019–3026 (2005).
  57. Poy MN, Eliasson L, Krutzfeldt J, Kuwajima S, Ma X, Macdonald PE, et al: A pancreatic islet-specific microRNA regulates insulin secretion. Nature 432:226–230 (2004).
  58. Reik W, Walter J: Genomic imprinting: parental influence on the genome. Nat Rev Genet 2:21–32 (2001).
  59. Robb GB, Brown KM, Khurana J, Rana TM: Specific and potent RNAi in the nucleus of human cells. Nat Struct Mol Biol 12:133–137 (2005).
  60. Runte M, Huttenhofer A, Gross S, Kiefmann M, Horsthemke B, Buiting K: The IC-SNURF- SNRPN transcript serves as a host for multiple small nucleolar RNA species and as an antisense RNA for UBE3A. Hum Mol Genet 10:2687–2700 (2001).
  61. Runte M, Varon R, Horn D, Horsthemke B, Buiting K: Exclusion of the C/D box snoRNA gene cluster HBII-52 from a major role in Prader-Willi syndrome. Hum Genet 116:228–230 (2005).
  62. Schule B, Albalwi M, Northrop E, Francis DI, Rowell M, Slater H, McKinlay Gardner RJ, Francke U: Molecular breakpoint cloning and gene expression studies of a novel translocation t(4;15) (q27;q11.2) associated with Prader-Willi syndrome. BMC Med Genet 6:18 (2005).
  63. Seitz H, Youngson N, Lin SP, Dalbert S, Paulsen M, Bachellerie JP, Ferguson-Smith AC, Cavaille J: Imprinted microRNA genes transcribed antisense to a reciprocally imprinted retrotransposon-like gene. Nat Genet 34:261–262 (2003).
  64. Seitz H, Royo H, Bortolin ML, Lin SP, Ferguson-Smith AC, Cavaille J: A large imprinted microRNA gene cluster at the mouse Dlk1-Gtl2 domain. Genome Res 14:1741–1748 (2004a).
  65. Seitz H, Royo H, Lin SP, Youngson N, Ferguson-Smith AC, Cavaille J: Imprinted small RNA genes. Biol Chem 385:905–911 (2004b).
  66. Sleutels F, Zwart R, Barlow DP: The non-coding Air RNA is required for silencing autosomal imprinted genes. Nature 415:810–813 (2002).
  67. Smit M, Segers K, Carrascosa LG, Shay T, Baraldi F, Gyapay G, et al: Mosaicism of Solid Gold supports the causality of a noncoding A-to-G transition in the determinism of the callipyge phenotype. Genetics 163:453–456 (2003).
  68. Svoboda P, Stein P, Filipowicz W, Schultz RM: Lack of homologous sequence-specific DNA methylation in response to stable dsRNA expression in mouse oocytes. Nucleic Acids Res 32:3601–3606 (2004).
  69. Tomari Y, Zamore PD: Perspective: machines for RNAi. Genes Dev 19:517–529 (2005).
  70. Vitali P, Basyuk E, Le Meur E, Bertrand E, Muscatelli F, Cavaille J, Huttenhofer A: ADAR2-mediated editing of RNA substrates in the nucleolus is inhibited by C/D small nucleolar RNAs. J Cell Biol 169:745–753 (2005).
  71. Wirth J, Back E, Huttenhofer A, Nothwang HG, Lich C, Gross S, et al: A translocation breakpoint cluster disrupts the newly defined 3′ end of the SNURF-SNRPN transcription unit on chromosome 15. Hum Mol Genet 10:201–210 (2001).
  72. Xie X, Lu J, Kulbokas EJ, Golub TR, Mootha V, Lindblad-Toh K, Lander ES, Kellis M: Systematic discovery of regulatory motifs in human promoters and 3′ UTRs by comparison of several mammals. Nature 434:338–345 (2005).
  73. Yekta S, Shih IH, Bartel DP: MicroRNA-directed cleavage of HOXB8 mRNA. Science 304:594–596 (2004).
  74. Youngson NA, Kocialkowski S, Peel N, Ferguson-Smith AC: A small family of sushi-class retrotransposon-derived genes in mammals and their relation to genomic imprinting. J Mol Evol 61:481–490 (2005).

Article / Publication Details

First-Page Preview
Abstract of Regulatory Mechanisms

Published online: March 30, 2006
Issue release date: March 2006

Number of Print Pages: 10
Number of Figures: 3
Number of Tables: 0

ISSN: 1424-8581 (Print)
eISSN: 1424-859X (Online)

For additional information: https://www.karger.com/CGR


Copyright / Drug Dosage / Disclaimer

Copyright: All rights reserved. No part of this publication may be translated into other languages, reproduced or utilized in any form or by any means, electronic or mechanical, including photocopying, recording, microcopying, or by any information storage and retrieval system, without permission in writing from the publisher.
Drug Dosage: The authors and the publisher have exerted every effort to ensure that drug selection and dosage set forth in this text are in accord with current recommendations and practice at the time of publication. However, in view of ongoing research, changes in government regulations, and the constant flow of information relating to drug therapy and drug reactions, the reader is urged to check the package insert for each drug for any changes in indications and dosage and for added warnings and precautions. This is particularly important when the recommended agent is a new and/or infrequently employed drug.
Disclaimer: The statements, opinions and data contained in this publication are solely those of the individual authors and contributors and not of the publishers and the editor(s). The appearance of advertisements or/and product references in the publication is not a warranty, endorsement, or approval of the products or services advertised or of their effectiveness, quality or safety. The publisher and the editor(s) disclaim responsibility for any injury to persons or property resulting from any ideas, methods, instructions or products referred to in the content or advertisements.