Skip to main content Accessibility help
×
Hostname: page-component-848d4c4894-4hhp2 Total loading time: 0 Render date: 2024-05-01T00:38:10.748Z Has data issue: false hasContentIssue false

5 - miRNAs in the brain and the application of RNAi to neurons

Published online by Cambridge University Press:  31 July 2009

Anna M. Krichevsky
Affiliation:
Department of Neurology and Center for Neurologic Diseases, Brigham and Women's Hospital, Harvard Medical School
Shih-Chu Kao
Affiliation:
Department of Neurology and Center for Neurologic Diseases, Brigham and Women's Hospital, Harvard Medical School
Li-Huei Tsai
Affiliation:
Department of Neurology and Center for Neurologic Diseases, Brigham and Women's Hospital, Harvard Medical School
Kenneth S. Kosik
Affiliation:
Department of Neurology and Center for Neurologic Diseases, Brigham and Women's Hospital, Harvard Medical School
Krishnarao Appasani
Affiliation:
GeneExpression Systems, Inc., Massachusetts
Andrew Fire
Affiliation:
Stanford University, California
Get access

Summary

miRNAs in the brain

Several hundred microRNAs (miRNAs) have been cloned from a wide range of organisms across phylogeny. miRNAs are 19–23 nucleotide transcripts with characteristic 3′ hydroxyl and 5′ phosphate termini cleaved from a ∼70-nt hairpin precursor by Dicer Ribonuclease III (Hütvagner et al., 2001; Ketting et al., 2001). Many miRNAs, often with highly conserved sequences, have been mapped in the genomes of C. elegans, Drosophila, rodents and humans (Lagos-Quintana et al., 2001; Lau et al., 2001; Lee and Ambros, 2001; Lagos-Quintana et al., 2002; Mourelatos et al., 2002; Dostie et al., 2003). Based on the length, hairpin structure and conservation the total number of miRNAs in the Drosophila genome has been estimated to be 110 (Lai et al., 2003) and in the human genome to be 255 (Lim et al., 2003). Some miRNAs are organized in the genome as clusters which can be separated by intervals as short as a few nucleotides (Lagos-Quintana et al., 2001; Lau et al., 2001). Despite the high degree of conservation of miRNAs, their functions in general, and in mammals particularly, have not been well defined. The first two miRNAs discovered, lin-4 and let-7, were found in C. elegans where they control developmental timing. These short transcripts form imperfect base pairing with elements within the 3′ UTR of target mRNAs and attenuate their translation (Lee et al., 1993; Wightman et al., 1993; Olsen and Ambros, 1999; Reinhart et al., 2000; Slack et al., 2000).

Type
Chapter
Information
RNA Interference Technology
From Basic Science to Drug Development
, pp. 84 - 100
Publisher: Cambridge University Press
Print publication year: 2005

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Aakalu, G., Smith, W. B., Nguyen, N., Jiang, C. and Schuman, E. M. (2001). Dynamic visualization of local protein synthesis in hippocampal neurons. Neuron, 30, 489–502CrossRefGoogle ScholarPubMed
Ambros, V. (2000). Control of developmental timing in Caenorhabditis elegans. Current Opinion in Genetics and Development, 10, 428–433CrossRefGoogle ScholarPubMed
Ambros, V., Lee, R. C., Lavanway, A., Williams, P. T. and Jewell, D. (2003). microRNAs and other tiny endogenous RNAs in C. elegans. Current Biology, 13, 807–818CrossRefGoogle ScholarPubMed
Basi, G., Frigon, N., Barbour, R., Doan, T., Gordon, G., McConlogue, L., Sinha, S. and Zeller, M. (2003). Antagonistic effects of beta-site amyloid precursor protein-cleaving enzymes 1 and 2 on beta-amyloid peptide production in cells. Journal of Biological Chemistry, 278, 31512–31520CrossRefGoogle ScholarPubMed
Baulcombe, D. (2002). DNA events. An RNA microcosm. Science, 297, 2002–2003CrossRefGoogle ScholarPubMed
Brennecke, J., Hipfner, D. R., Stark, A., Russell, R. B. and Cohen, S. M. (2003). Bantam encodes a developmentally regulated microRNA that controls cell proliferation and regulates the proapoptotic gene hid in Drosophila. Cell, 113, 25–36CrossRefGoogle ScholarPubMed
Caceres, A., Mautino, J. and Kosik, K. S. (1992). Suppression of MAP-2 in cultured cerebellar macroneurons inhibits minor neurite formation. Neuron, 9, 607–618CrossRefGoogle Scholar
Carrington, J. C. and Ambros, V. (2003). Role of microRNAs in plant and animal development. Science, 301, 336–338CrossRefGoogle ScholarPubMed
Chen, C. Z., Li, L., Lodish, H. F. and Bartel, D. P. (2004). microRNAs modulate hematopoietic lineage differentiation. Science, 2;303(5654):83–6CrossRefGoogle ScholarPubMed
Doench, J. G., Petersen, C. P. and Sharp, P. A. (2003). siRNAs can function as miRNAs. Genes & Development, 17, 438–442CrossRefGoogle ScholarPubMed
Dostie, J., Mourelatos, Z., Yang, M., Sharma, A. and Dreyfuss, G. (2003). Numerous microRNPs in neuronal cells containing novel microRNAs. RNA, 9, 180–186CrossRefGoogle ScholarPubMed
Eberwine, J., Miyashiro, K., Kacharmina, J. E. and Job, C. (2001). Local translation of classes of mRNAs that are targeted to neuronal dendrites. Proceedings of the National Academy of Sciences USA, 98, 7080–7085CrossRefGoogle ScholarPubMed
Elbashir, S. M., Martinez, J., Patkaniowska, A., Lendeckel, W. and Tuschl, T. (2001). Functional anatomy of siRNAs for mediating efficient RNAi in Drosophila melanogaster embryo lysate. European Molecular Biology Organization Journal, 20, 6877–6888CrossRefGoogle ScholarPubMed
Farzan, M., Schnitzler, C. E., Vasilieva, N., Leung, D. and Choe, H. (2000). BACE2, a beta –secretase homolog, cleaves at the beta site and within the amyloid-beta region of the amyloid-beta precursor protein. Proceedings of the National Academy of Sciences USA, 97, 9712–9717CrossRefGoogle ScholarPubMed
Fink, C. C., Bayer, K. U., Myers, J. W., Ferrell, J. E. Jr., Schulman, H. and Meyer, T. (2003). Selective regulation of neurite extension and synapse formation by the beta but not the alpha isoform of CaMKII. Neuron, 39, 283–297CrossRefGoogle Scholar
Fukumoto, H., Cheung, B. S., Hyman, B. T. and Irizarry, M. C. (2002). Beta-secretase protein and activity are increased in the neocortex in Alzheimer disease. Archives of Neurology, 59, 1381–1389CrossRefGoogle ScholarPubMed
Gaudilliere, B., Shi, Y. and Bonni, A. (2002). RNA interference reveals a requirement for myocyte enhancer factor 2A in activity-dependent neuronal survival. Journal of Biological Chemistry, 277, 46442–46446CrossRefGoogle ScholarPubMed
Golub, A. M., Masiarz, F. R., Villars, T. and McConnell, J. V. (1970). Incubation effects in behavior induction in rats. Science, 168, 392–395CrossRefGoogle ScholarPubMed
Gonzalez-Billault, C., Engelke, M., Jimenez-Mateos, E. M., Wandosell, F., Caceres, A. and Avila, J. (2002). Participation of structural microtubule-associated proteins (MAPs) in the development of neuronal polarity. Journal of Neuroscience Research, 67, 713–719CrossRefGoogle ScholarPubMed
Grishok, A., Pasquinelli, A. E., Conte, D., Li, N., Parrish, S., Ha, I., Baillie, D. L., Fire, A., Ruvkun, G. and Mello, C. C. (2001). Genes and mechanisms related to RNA interference regulate expression of the small temporal RNAs that control C. elegans developmental timing. Cell, 106, 23–34CrossRefGoogle ScholarPubMed
Hallam, S. J. and Jin, Y. (1998). lin-14 regulates the timing of synaptic remodelling in Caenorhabditis elegans. Nature, 395, 78–82CrossRefGoogle ScholarPubMed
Handler, M., Yang, X. and Shen, J. (2000). Presenilin-1 regulates neuronal differentiation during neurogenesis. Development, 127, 2593–2606Google ScholarPubMed
Hardy, J. A. and Higgins, G. A. (1992). Alzheimer's disease: The amyloid cascade hypothesis. Science, 256, 184–185CrossRefGoogle ScholarPubMed
Holsinger, R. M., McLean, C. A., Beyreuther, K., Masters, C. L. and Evin, G. (2002). Increased expression of the amyloid precursor beta-secretase in Alzheimer's disease. Annals of Neurology, 51, 783–786CrossRefGoogle ScholarPubMed
Hütvagner, G., McLachlan, J., Pasquinelli, A. E., Balint, E., Tuschl, T. and Zamore, P. D. (2001). A cellular function for the RNA-interference enzyme Dicer in the maturation of the let-7 small temporal RNA. Science, 293, 834–838CrossRefGoogle ScholarPubMed
Kao, S. C., Krichevsky, A. M., Kosik, K. S. and Tsai, L. H. (2003). BACE1 suppression by RNA interference in primary cortical neurons. Journal of Biological Chemistry, 279, 1942–1949CrossRefGoogle ScholarPubMed
Kasschau, K. D., Xie, Z., Allen, E., Llave, C., Chapman, E. J., Krizan, K. A. and Carrington, J. C. (2003). P1/HC-Pro, a viral suppressor of RNA silencing, interferes with Arabidopsis development and miRNA unction. Developmental Cell, 4, 205–217CrossRefGoogle ScholarPubMed
Ketting, R. F., Fischer, S. E., Bernstein, E., Sijen, T., Hannon, G. J. and Plasterk, R. H. (2001). Dicer functions in RNA interference and in synthesis of small RNA involved in developmental timing in C. elegans. Genes & Development, 15, 2654–2659CrossRefGoogle ScholarPubMed
Kim, J, Krichevsky, A, Grad, Y, Hayes, G. D., Kosik, K. S., Church, G. M., Ruvkun, G. (2004). Identification of many microRNAs that copurify with polyribosomes in mammalian neurons. Proc Natl Acad Sci USA. Jan 6;101(1):360–5CrossRefGoogle ScholarPubMed
Krichevsky, A. M. and Kosik, K. S. (2001). Neuronal RNA granules: A link between RNA localization and stimulation-dependent translation. Neuron, 32, 683–696CrossRefGoogle ScholarPubMed
Krichevsky, A. M. and Kosik, K. S. (2002). RNAi functions in cultured mammalian neurons. Proceedings of the National Academy of Sciences USA, 99, 11926–11929CrossRefGoogle ScholarPubMed
Krichevsky, A. M., King, K. S., Donahue, C. P., Khrapko, K. and Kosik, K. S. (2003). A microRNA array reveals extensive regulation of microRNAs during brain development. RNA, 9, 1274–1281CrossRefGoogle ScholarPubMed
Lagos-Quintana, M., Rauhut, R., Lendeckel, W. and Tuschl, T. (2001). Identification of novel genes coding for small expressed RNAs. Science, 294, 853–858CrossRefGoogle ScholarPubMed
Lagos-Quintana, M, , R. R., Yalcin, A, Meyer, J, Lendeckel, W. and Tuschl, T. (2002). Identification of tissue-specific MicroRNA's from mouse. Current Biology, 12, 735–739CrossRefGoogle Scholar
Lai, E. C., Tomancak, P., Williams, R. W. and Rubin, G. M. (2003). Computational identification of Drosophila microRNA genes. Genome Biology, 4, R42CrossRefGoogle ScholarPubMed
Lau, N. C., Lim, L. P., Weinstein, E. G. and Bartel, D. P. (2001). An abundant class of tiny RNAs with probable regulatory roles in Caenorhabditis elegans. Science, 294, 858–862CrossRefGoogle ScholarPubMed
Lee, R. C. and Ambros, V. (2001). An extensive class of small RNAs in Caenorhabditis elegans. Science, 294, 862–864CrossRefGoogle ScholarPubMed
Lee, R. C., Feinbaum, R. L. and Ambros, V. (1993). The C. elegans heterochronic gene lin-4 encodes small RNAs with antisense complementarity to lin-14. Cell, 75, 843–854CrossRefGoogle Scholar
Lee, Y., Ahn, C., Han, J., Choi, H., Kim, J., Yim, J., Lee, J., Provost, P., Radmark, O., Kim, S. and Kim, V. N. (2003). The nuclear RNase III Drosha initiates microRNA processing. Nature, 425, 415–419CrossRefGoogle ScholarPubMed
Lim, L. P., Glasner, M. E., Yekta, S., Burge, C. B. and Bartel, D. P. (2003). Vertebrate microRNA genes. Science, 299, 1540CrossRefGoogle ScholarPubMed
Luo, Y., Bolon, B., Kahn, S., Bennett, B. D., Babu-Khan, S., Denis, P., Fan, W., Kha, H., Zhang, J., Gong, Y., et al. (2001). Mice deficient in BACE1, the Alzheimer's beta-secretase, have normal phenotype and abolished beta-amyloid generation. Nature Neuroscience, 4, 231–232CrossRefGoogle ScholarPubMed
McConnell, J. V. (1966). Comparative physiology: learning in invertebrates. Annual Reviews of Physiology, 28, 107–136CrossRefGoogle ScholarPubMed
Miller, S., Yasuda, M., Coats, J. K., Jones, Y., Martone, M. E. and Mayford, M. (2002). Disruption of dendritic translation of CaMKIIalpha impairs stabilization of synaptic plasticity and memory consolidation. Neuron, 36, 507–519CrossRefGoogle ScholarPubMed
Misonou, H., Morishima-Kawashima, M. and Ihara, Y. (2000). Oxidative stress induces intracellular accumulation of amyloid beta-protein (Abeta) in human neuroblastoma cells. Biochemistry, 39, 6951–6959CrossRefGoogle Scholar
Mourelatos, Z., Dostie, J., Paushkin, S., Sharma, A., Charroux, B., Abel, L., Rappsilber, J., Mann, M. and Dreyfuss, G. (2002). miRNPs: a novel class of ribonucleoproteins containing numerous microRNAs. Genes & Development, 16, 720–728CrossRefGoogle ScholarPubMed
O'Donnell, W. T. and Warren, S. T. (2002). A decade of molecular studies of Fragile X syndrome. Annual Reviews of Neuroscience, 25, 315–338CrossRefGoogle ScholarPubMed
Okabe, M., Imai, T., Kurusu, M., Hiromi, Y. and Okano, H. (2001). Translational repression determines a neuronal potential in Drosophila asymmetric cell division. Nature, 411, 94–98CrossRefGoogle ScholarPubMed
Olsen, P. H. and Ambros, V. (1999). The lin-4 regulatory RNA controls developmental timing in Caenorhabditis elegans by blocking LIN-14 protein synthesis after the initiation of translation. Developmental Biology, 216, 671–680CrossRefGoogle ScholarPubMed
Price, D. L., Sisodia, S. S. and Gandy, S. E. (1995). Amyloid beta amyloidosis in Alzheimer's disease. Current Opinion in Neurology, 8, 268–274CrossRefGoogle ScholarPubMed
Price, D. L., Tanzi, R. E., Borchelt, D. R. and Sisodia, S. S. (1998). Alzheimer's disease: Genetic studies and transgenic models. Annual Reviews of Genetics, 32, 461–493CrossRefGoogle ScholarPubMed
Reinhart, B. J., Slack, F. J., Basson, M., Pasquinelli, A. E., Bettinger, J. C., Rougvie, A. E., Horvitz, H. R. and Ruvkun, G. (2000). The 21-nucleotide let-7 RNA regulates developmental timing in Caenorhabditis elegans. Nature, 403, 901–906CrossRefGoogle ScholarPubMed
Roberds, S. L., Anderson, J., Basi, G., Bienkowski, M. J., Branstetter, D. G., Chen, K. S., Freedman, S. B., Frigon, N. L., Games, D., Hu, K., et al. (2001). BACE knockout mice are healthy despite lacking the primary beta-secretase activity in brain: Implications for Alzheimer's disease therapeutics. Human Molecular Genetics, 10, 1317–1324CrossRefGoogle ScholarPubMed
Selkoe, D. J. (2000). Toward a comprehensive theory for Alzheimer's disease. Hypothesis: Alzheimer's disease is caused by the cerebral accumulation and cytotoxicity of amyloid beta-protein. Annals of New York Academy of Sciences, 924, 17–25CrossRefGoogle Scholar
Shen, J., Bronson, T., Chjen, D. F., Xia, W., Selkoe, D. J. and Tonegawa, S. (1997). Skeletal and CNS defects in presenilin-1-deficient mice. Cell, 89, 629–639CrossRefGoogle ScholarPubMed
Slack, F. J., Basson, M., Liu, Z., Ambros, V., Horvitz, H. R. and Ruvkun, G. (2000). The lin-41 RBCC gene acts in the C. elegans heterochronic pathway between the let-7 regulatory RNA and the LIN-29 transcription factor. Molecular Cell, 5, 659–669CrossRefGoogle Scholar
Steward, O. and Schuman, E. M. (2001). Protein synthesis at synaptic sites on dendrites. Annual Reviews of Neuroscience, 24, 299–325CrossRefGoogle ScholarPubMed
Tamagno, E., Bardini, P., Obbili, A., Vitali, A., Borghi, R., Zaccheo, D., Pronzato, M. A., Danni, O., Smith, M. A., Perry, G. and Tabaton, M. (2002). Oxidative stress increases expression and activity of BACE in NT2 neurons. Neurobiology Disorders, 10, 279–288CrossRefGoogle ScholarPubMed
Timmons, L., Court, D. L. and Fire, A. (2001). Ingestion of bacterially expressed dsRNAs can produce specific and potent genetic interference in Caenorhabditis elegans. Gene, 263, 103–112CrossRefGoogle ScholarPubMed
Whitehouse, P. J., Struble, R. G., Hedreen, J. C., Clark, A. W. and Price, D. L. (1985). Alzheimer's disease and related dementias: Selective involvement of specific neuronal systems. Critical Reviews of Clinical Neurobiology, 1, 319–339Google ScholarPubMed
Wienholds, E., Koudijs, M. J., Eeden, F. J., Cuppen, E. and Plasterk, R. H. (2003). The microRNA-producing enzyme Dicer1 is essential for zebrafish development. Nature Genetics, 35, 217–218CrossRefGoogle ScholarPubMed
Wightman, B., Ha, I. and Ruvkun, G. (1993). Posttranscriptional regulation of the heterochronic gene lin-14 by lin-4 mediates temporal pattern formation in C. elegans. Cell, 75, 855–862CrossRefGoogle ScholarPubMed
Yan, R., Munzner, J. B., Shuck, M. E. and Bienkowski, M. J. (2001). BACE2 functions as an alternative alpha-secretase in cells. Journal of Biological Chemistry, 276, 34019–34027CrossRefGoogle ScholarPubMed
Yang, L. B., Lindholm, K., Yan, R., Citron, M., Xia, W., Yang, X. L., Beach, T., Sue, L., Wong, P., Price, D., et al. (2003). Elevated beta-secretase expression and enzymatic activity detected in sporadic Alzheimer disease. Nature Medicine, 9, 3–4CrossRefGoogle ScholarPubMed
Zeng, Y., Yi, R. and Cullen, B. R. (2003). microRNAs and small interfering RNAs can inhibit mRNA expression by similar mechanisms. Proceedings of the National Academy of Sciences USA, 100, 9779–9784CrossRefGoogle ScholarPubMed

Save book to Kindle

To save this book to your Kindle, first ensure coreplatform@cambridge.org is added to your Approved Personal Document E-mail List under your Personal Document Settings on the Manage Your Content and Devices page of your Amazon account. Then enter the ‘name’ part of your Kindle email address below. Find out more about saving to your Kindle.

Note you can select to save to either the @free.kindle.com or @kindle.com variations. ‘@free.kindle.com’ emails are free but can only be saved to your device when it is connected to wi-fi. ‘@kindle.com’ emails can be delivered even when you are not connected to wi-fi, but note that service fees apply.

Find out more about the Kindle Personal Document Service.

  • miRNAs in the brain and the application of RNAi to neurons
    • By Anna M. Krichevsky, Department of Neurology and Center for Neurologic Diseases, Brigham and Women's Hospital, Harvard Medical School, Shih-Chu Kao, Department of Neurology and Center for Neurologic Diseases, Brigham and Women's Hospital, Harvard Medical School, Li-Huei Tsai, Department of Neurology and Center for Neurologic Diseases, Brigham and Women's Hospital, Harvard Medical School, Kenneth S. Kosik, Department of Neurology and Center for Neurologic Diseases, Brigham and Women's Hospital, Harvard Medical School
  • Edited by Krishnarao Appasani, GeneExpression Systems, Inc., Massachusetts
  • Foreword by Andrew Fire, Stanford University, California, Marshall Nirenberg
  • Book: RNA Interference Technology
  • Online publication: 31 July 2009
  • Chapter DOI: https://doi.org/10.1017/CBO9780511546402.008
Available formats
×

Save book to Dropbox

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Dropbox.

  • miRNAs in the brain and the application of RNAi to neurons
    • By Anna M. Krichevsky, Department of Neurology and Center for Neurologic Diseases, Brigham and Women's Hospital, Harvard Medical School, Shih-Chu Kao, Department of Neurology and Center for Neurologic Diseases, Brigham and Women's Hospital, Harvard Medical School, Li-Huei Tsai, Department of Neurology and Center for Neurologic Diseases, Brigham and Women's Hospital, Harvard Medical School, Kenneth S. Kosik, Department of Neurology and Center for Neurologic Diseases, Brigham and Women's Hospital, Harvard Medical School
  • Edited by Krishnarao Appasani, GeneExpression Systems, Inc., Massachusetts
  • Foreword by Andrew Fire, Stanford University, California, Marshall Nirenberg
  • Book: RNA Interference Technology
  • Online publication: 31 July 2009
  • Chapter DOI: https://doi.org/10.1017/CBO9780511546402.008
Available formats
×

Save book to Google Drive

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Google Drive.

  • miRNAs in the brain and the application of RNAi to neurons
    • By Anna M. Krichevsky, Department of Neurology and Center for Neurologic Diseases, Brigham and Women's Hospital, Harvard Medical School, Shih-Chu Kao, Department of Neurology and Center for Neurologic Diseases, Brigham and Women's Hospital, Harvard Medical School, Li-Huei Tsai, Department of Neurology and Center for Neurologic Diseases, Brigham and Women's Hospital, Harvard Medical School, Kenneth S. Kosik, Department of Neurology and Center for Neurologic Diseases, Brigham and Women's Hospital, Harvard Medical School
  • Edited by Krishnarao Appasani, GeneExpression Systems, Inc., Massachusetts
  • Foreword by Andrew Fire, Stanford University, California, Marshall Nirenberg
  • Book: RNA Interference Technology
  • Online publication: 31 July 2009
  • Chapter DOI: https://doi.org/10.1017/CBO9780511546402.008
Available formats
×