Endogenous retroviruses and retrotransposons contribute functional genetic variation in animal genomes. In mice, Intracisternal A Particles (IAPs) are a frequent source of both new mutations and polymorphism across laboratory strains. Intronic IAPs can induce alternative RNA processing choices, including alternative splicing. We previously showed IAP I?1 subfamily insertional mutations are suppressed by a wild-derived allele of the major mRNA export factor, Nxf1. Here we show that a wider diversity of IAP insertions present in the mouse reference sequence induce insertion-dependent alternative processing that is suppressed by Nxf1CAST alleles. These insertions typically show more modest gene expression changes than de novo mutations, suggesting selection or attenuation. Genome-wide splicing-sensitive microarrays and gene-focused assays confirm specificity of Nxf1 genetic modifier activity for IAP insertion alleles. Strikingly, CRISPR/Cas9-mediated genome editing demonstrates that a single amino acid substitution in Nxf1, E610G, is sufficient to recreate a quantitative genetic modifier in a co-isogenic background.
References
[1]
Cowley M, Oakey RJ. Transposable elements re-wire and fine-tune the transcriptome. PLoS genetics. 2013;9(1):e1003234. Epub 2013/01/30. doi: 10.1371/journal.pgen.1003234. pmid:23358118
[2]
Gifford WD, Pfaff SL, Macfarlan TS. Transposable elements as genetic regulatory substrates in early development. Trends Cell Biol. 2013;23(5):218–26. Epub 2013/02/16. doi: 10.1016/j.tcb.2013.01.001. pmid:23411159
[3]
Peter IS, Davidson EH. Evolution of gene regulatory networks controlling body plan development. Cell. 2011;144(6):970–85. Epub 2011/03/19. doi: 10.1016/j.cell.2011.02.017. pmid:21414487
[4]
Waterston RH, Lindblad-Toh K, Birney E, Rogers J, Abril JF, Agarwal P, et al. Initial sequencing and comparative analysis of the mouse genome. Nature. 2002;420(6915):520–62. pmid:12466850
[5]
Hamilton BA, Frankel WN. Of mice and genome sequence. Cell. 2001;107(1):13–6. pmid:11595181 doi: 10.1016/s0092-8674(01)00514-1
[6]
Maksakova IA, Romanish MT, Gagnier L, Dunn CA, van de Lagemaat LN, Mager DL. Retroviral elements and their hosts: insertional mutagenesis in the mouse germ line. PLoS genetics. 2006;2(1):e2. pmid:16440055 doi: 10.1371/journal.pgen.0020002
[7]
Vasicek TJ, Zeng L, Guan XJ, Zhang T, Costantini F, Tilghman SM. Two dominant mutations in the mouse fused gene are the result of transposon insertions. Genetics. 1997;147(2):777–86. pmid:9335612
[8]
Duhl DM, Vrieling H, Miller KA, Wolff GL, Barsh GS. Neomorphic agouti mutations in obese yellow mice. Nature Genet. 1994;8(1):59–65. pmid:7987393 doi: 10.1038/ng0994-59
[9]
Lugani F, Arora R, Papeta N, Patel A, Zheng Z, Sterken R, et al. A retrotransposon insertion in the 5' regulatory domain of Ptf1a results in ectopic gene expression and multiple congenital defects in Danforth's short tail mouse. PLoS genetics. 2013;9(2):e1003206. Epub 2013/02/26. doi: 10.1371/journal.pgen.1003206. pmid:23437001
[10]
Semba K, Araki K, Matsumoto K, Suda H, Ando T, Sei A, et al. Ectopic expression of Ptf1a induces spinal defects, urogenital defects, and anorectal malformations in Danforth's short tail mice. PLoS genetics. 2013;9(2):e1003204. Epub 2013/02/26. doi: 10.1371/journal.pgen.1003204. pmid:23436999
[11]
Vlangos CN, Siuniak AN, Robinson D, Chinnaiyan AM, Lyons RH Jr., Cavalcoli JD, et al. Next-generation sequencing identifies the Danforth's short tail mouse mutation as a retrotransposon insertion affecting Ptf1a expression. PLoS genetics. 2013;9(2):e1003205. Epub 2013/02/26. doi: 10.1371/journal.pgen.1003205. pmid:23437000
[12]
Bentley DL. Coupling mRNA processing with transcription in time and space. Nat Rev Genet. 2014;15(3):163–75. Epub 2014/02/12. doi: 10.1038/nrg3662. pmid:24514444
[13]
Auboeuf D, Honig A, Berget SM, O'Malley BW. Coordinate regulation of transcription and splicing by steroid receptor coregulators. Science. 2002;298(5592):416–9. pmid:12376702 doi: 10.1126/science.1073734
[14]
Cramer P, Pesce CG, Baralle FE, Kornblihtt AR. Functional association between promoter structure and transcript alternative splicing. Proc Natl Acad Sci U S A. 1997;94(21):11456–60. Epub 1997/10/23. pmid:9326631 doi: 10.1073/pnas.94.21.11456
[15]
Kornblihtt AR. Promoter usage and alternative splicing. Curr Opin Cell Biol. 2005;17(3):262–8. pmid:15901495 doi: 10.1016/j.ceb.2005.04.014
[16]
de la Mata M, Kornblihtt AR. RNA polymerase II C-terminal domain mediates regulation of alternative splicing by SRp20. Nature structural & molecular biology. 2006;13(11):973–80. doi: 10.1038/nsmb1155
[17]
Kornblihtt AR. Chromatin, transcript elongation and alternative splicing. Nature structural & molecular biology. 2006;13(1):5–7. doi: 10.1038/nsmb0106-5
[18]
Vargas DY, Shah K, Batish M, Levandoski M, Sinha S, Marras SA, et al. Single-molecule imaging of transcriptionally coupled and uncoupled splicing. Cell. 2011;147(5):1054–65. Epub 2011/11/29. doi: 10.1016/j.cell.2011.10.024. pmid:22118462
[19]
Concepcion D, Flores-Garcia L, Hamilton BA. Multipotent genetic suppression of retrotransposon-induced mutations by Nxf1 through fine-tuning of alternative splicing. PLoS genetics. 2009;5(5):e1000484. doi: 10.1371/journal.pgen.1000484. pmid:19436707
[20]
Floyd JA, Gold DA, Concepcion D, Poon TH, Wang X, Keithley E, et al. A natural allele of Nxf1 suppresses retrovirus insertional mutations. Nature Genetics. 2003;35:221–8. pmid:14517553 doi: 10.1038/ng1247
[21]
Kuff EL, Lueders KK. The intracisternal A-particle gene family: structure and functional aspects. Advances in cancer research. 1988;51:183–276. pmid:3146900 doi: 10.1016/s0065-230x(08)60223-7
[22]
Fujikawa K, Suzuki H, McMullen B, Chung D. Purification of human von Willebrand factor-cleaving protease and its identification as a new member of the metalloproteinase family. Blood. 2001;98(6):1662–6. pmid:11535495 doi: 10.1182/blood.v98.6.1662
[23]
Gerritsen HE, Robles R, Lammle B, Furlan M. Partial amino acid sequence of purified von Willebrand factor-cleaving protease. Blood. 2001;98(6):1654–61. pmid:11535494 doi: 10.1182/blood.v98.6.1654
[24]
Levy GG, Nichols WC, Lian EC, Foroud T, McClintick JN, McGee BM, et al. Mutations in a member of the ADAMTS gene family cause thrombotic thrombocytopenic purpura. Nature. 2001;413(6855):488–94. pmid:11586351 doi: 10.1038/35097008
[25]
Nolasco LH, Turner NA, Bernardo A, Tao Z, Cleary TG, Dong JF, et al. Hemolytic uremic syndrome-associated Shiga toxins promote endothelial-cell secretion and impair ADAMTS13 cleavage of unusually large von Willebrand factor multimers. Blood. 2005;106(13):4199–209. pmid:16131569 doi: 10.1182/blood-2005-05-2111
[26]
Fujioka M, Hayakawa K, Mishima K, Kunizawa A, Irie K, Higuchi S, et al. ADAMTS13 gene deletion aggravates ischemic brain damage: a possible neuroprotective role of ADAMTS13 by ameliorating postischemic hypoperfusion. Blood. 2010;115(8):1650–3. doi: 10.1182/blood-2009-06-230110. pmid:19965676
[27]
Banno F, Kaminaka K, Soejima K, Kokame K, Miyata T. Identification of strain-specific variants of mouse Adamts13 gene encoding von Willebrand factor-cleaving protease. J Biol Chem. 2004;279(29):30896–903. pmid:15136581 doi: 10.1074/jbc.m314184200
[28]
Uemura M, Tatsumi K, Matsumoto M, Fujimoto M, Matsuyama T, Ishikawa M, et al. Localization of ADAMTS13 to the stellate cells of human liver. Blood. 2005;106(3):922–4. pmid:15855280 doi: 10.1182/blood-2005-01-0152
[29]
Zhou W, Inada M, Lee TP, Benten D, Lyubsky S, Bouhassira EE, et al. ADAMTS13 is expressed in hepatic stellate cells. Laboratory investigation; a journal of technical methods and pathology. 2005;85(6):780–8. pmid:15806136 doi: 10.1038/labinvest.3700275
[30]
Zhang Y, Romanish MT, Mager DL. Distributions of transposable elements reveal hazardous zones in mammalian introns. PLoS Comput Biol. 2011;7(5):e1002046. Epub 2011/05/17. doi: 10.1371/journal.pcbi.1002046. pmid:21573203
[31]
Zhang Y, Maksakova IA, Gagnier L, van de Lagemaat LN, Mager DL. Genome-Wide Assessments Reveal Extremely High Levels of Polymorphism of Two Active Families of Mouse Endogenous Retroviral Elements. PLoS genetics. 2008;4(2):e1000007 doi: 10.1371/journal.pgen.1000007. pmid:18454193
[32]
Yalcin B, Wong K, Agam A, Goodson M, Keane TM, Gan X, et al. Sequence-based characterization of structural variation in the mouse genome. Nature. 2011;477(7364):326–9. Epub 2011/09/17. doi: 10.1038/nature10432. pmid:21921916
[33]
Keane TM, Goodstadt L, Danecek P, White MA, Wong K, Yalcin B, et al. Mouse genomic variation and its effect on phenotypes and gene regulation. Nature. 2011;477(7364):289–94. Epub 2011/09/17. doi: 10.1038/nature10413. pmid:21921910
[34]
Barash Y, Calarco JA, Gao W, Pan Q, Wang X, Shai O, et al. Deciphering the splicing code. Nature. 2010;465(7294):53–9. doi: 10.1038/nature09000. pmid:20445623
[35]
Huelga SC, Vu AQ, Arnold JD, Liang TY, Liu PP, Yan BY, et al. Integrative genome-wide analysis reveals cooperative regulation of alternative splicing by hnRNP proteins. Cell reports. 2012;1(2):167–78. Epub 2012/05/11. doi: 10.1016/j.celrep.2012.02.001. pmid:22574288
[36]
Du H, Cline MS, Osborne RJ, Tuttle DL, Clark TA, Donohue JP, et al. Aberrant alternative splicing and extracellular matrix gene expression in mouse models of myotonic dystrophy. Nature structural & molecular biology. 2010;17(2):187–93. Epub 2010/01/26. doi: 10.1038/nsmb.1720.
[37]
Gehman LT, Stoilov P, Maguire J, Damianov A, Lin CH, Shiue L, et al. The splicing regulator Rbfox1 (A2BP1) controls neuronal excitation in the mammalian brain. Nat Genet. 2011;43(7):706–11. Epub 2011/05/31. doi: 10.1038/ng.841. pmid:21623373
[38]
Lagier-Tourenne C, Polymenidou M, Hutt KR, Vu AQ, Baughn M, Huelga SC, et al. Divergent roles of ALS-linked proteins FUS/TLS and TDP-43 intersect in processing long pre-mRNAs. Nature neuroscience. 2012;15(11):1488–97. Epub 2012/10/02. doi: 10.1038/nn.3230. pmid:23023293
[39]
Polymenidou M, Lagier-Tourenne C, Hutt KR, Huelga SC, Moran J, Liang TY, et al. Long pre-mRNA depletion and RNA missplicing contribute to neuronal vulnerability from loss of TDP-43. Nature neuroscience. 2011;14(4):459–68. Epub 2011/03/02. doi: 10.1038/nn.2779. pmid:21358643
[40]
Wang H, Yang H, Shivalila CS, Dawlaty MM, Cheng AW, Zhang F, et al. One-step generation of mice carrying mutations in multiple genes by CRISPR/Cas-mediated genome engineering. Cell. 2013;153(4):910–8. Epub 2013/05/07. doi: 10.1016/j.cell.2013.04.025. pmid:23643243
[41]
Ran FA, Hsu PD, Wright J, Agarwala V, Scott DA, Zhang F. Genome engineering using the CRISPR-Cas9 system. Nature protocols. 2013;8(11):2281–308. Epub 2013/10/26. doi: 10.1038/nprot.2013.143. pmid:24157548
[42]
Hamilton BA, Yu BD. Modifier genes and the plasticity of genetic networks in mice. PLoS genetics. 2012;8(4):e1002644. Epub 2012/04/19. doi: 10.1371/journal.pgen.1002644. pmid:22511884
[43]
Li J, Akagi K, Hu Y, Trivett AL, Hlynialuk CJ, Swing DA, et al. Mouse endogenous retroviruses can trigger premature transcriptional termination at a distance. Genome Res. 2012;22(5):870–84. Epub 2012/03/01. doi: 10.1101/gr.130740.111. pmid:22367191
[44]
Zhou W, Bouhassira EE, Tsai HM. An IAP retrotransposon in the mouse ADAMTS13 gene creates ADAMTS13 variant proteins that are less effective in cleaving von Willebrand factor multimers. Blood. 2007;110(3):886–93. pmid:17426255 doi: 10.1182/blood-2007-01-070953
[45]
Nellaker C, Keane TM, Yalcin B, Wong K, Agam A, Belgard TG, et al. The genomic landscape shaped by selection on transposable elements across 18 mouse strains. Genome Biol. 2012;13(6):R45. Epub 2012/06/19. doi: 10.1186/gb-2012-13-6-r45. pmid:22703977
[46]
Banno F, Chauhan AK, Kokame K, Yang J, Miyata S, Wagner DD, et al. The distal carboxyl-terminal domains of ADAMTS13 are required for regulation of in vivo thrombus formation. Blood. 2009;113(21):5323–9. doi: 10.1182/blood-2008-07-169359. pmid:19109562
[47]
Hamilton BA, Smith DJ, Mueller KL, Kerrebrock AW, Bronson RT, van Berkel V, et al. The vibrator mutation causes neurodegeneration via reduced expression of PITP alpha: positional complementation cloning and extragenic suppression. Neuron. 1997;18(5):711–22. pmid:9182797 doi: 10.1016/s0896-6273(00)80312-8
[48]
Giardine B, Riemer C, Hardison RC, Burhans R, Elnitski L, Shah P, et al. Galaxy: a platform for interactive large-scale genome analysis. Genome Res. 2005;15(10):1451–5. Epub 2005/09/20. doi: 10.1101/gr.4086505. pmid:16169926
[49]
Rozen S, Skaletsky H. Primer3 on the WWW for general users and for biologist programmers. Methods in molecular biology (Clifton, NJ. 2000;132:365–86. pmid:10547847 doi: 10.1385/1-59259-192-2:365
[50]
Vandesompele J, De Preter K, Pattyn F, Poppe B, Van Roy N, De Paepe A, et al. Accurate normalization of real-time quantitative RT-PCR data by geometric averaging of multiple internal control genes. Genome biology. 2002;3(7):RESEARCH0034. Epub 2002/08/20. pmid:12184808 doi: 10.1186/gb-2002-3-7-research0034