Abstract
Transposable elements (TEs) have exerted an impact on genome evolution that is at once substantial and fundamental. They have promoted phenotypic diversity because of their potential for effecting genetic alteration in a great variety of settings and with significant magnitude. Both ancient and omnipresent, TEs can benefit lineages while simultaneously proving detrimental to some individuals. Transposable elements play reformatting, building, and sculpting roles as they effect changes in the genome through both direct and indirect means. Thus, their impact on soil microbes can be substantial. As short DNA sequences, TEs possess the capability to migrate between diverse sites within the genome, a capacity that enables them to promote genomic mutations in a number of ways, ranging from the most limited regulatory mutations to the most extensive rearrangements of the genome. Scientists who pioneered the original discovery of TEs announced their potential roles in genomic adaptation, which was sharply contested by other theorists. Such was the misunderstanding of the beneficial roles of TEs that for over two decades they were regarded almost exclusively in a negative light as genome-damaging intragenomic parasites. A major watershed in TE research came when the Drosophila melanogaster genome was sequenced, which unleashed unprecedented analysis of TEs. This path breaking investigation resulted in the initial identification of TE-produced adaptations in Drosophila melanogaster. Subsequent studies illuminated the fundamental contributions of TEs in the processes of adaptive evolution. This important inference was the product of a methodical search of the entire genome that focused on adaptive insertions that resulted from TEs.
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
References
Agudelo-Romero P, Carbonell P, Perez-Amador MA, Elena SF (2008) Virus adaptation by manipulation of host’s gene expression. PLoS ONE 3:e2397
Allavena P, Chieppa M, Monti P, Piemonti L (2004) From pattern recognition receptor to regulator of homeostasis: the double-faced macrophage mannose receptor. Crit Rev Immunol 24(3):179–192
Amemiya CT, Saha NR, Zapata A (2007) Evolution and development of immunological structures in the Lamprey. Curr Opin Immunol 19(5):535–541
Arnaud F, Caporale M, Varela M, Biek R, Chessa B, Alberti A, Golder M, Mura M, Zhang YP, Yu L, Pereira F, Demartini JC, Leymaster K, Spencer TE, Palmarini M (2007) A paradigm for virus-host coevolution: sequential counter-adaptations between endogenous and exogenous retroviruses. PLoS Pathog 3:e170
Bagasra O (2008) Role of mutually homologous microRNAs in HIV-1 inhibition. 33rd FEBS Congress & 11th IUBMB Conference, Athens, Greece, PP5A-1
Bagasra O (2006) A unified concept of HIV-1 latency. Expert Opin Biol Ther 6:1135–1149
Bagasra O (2005) RNAi as an anti-viral therapy. Expert Opin Biol Ther 5(11):1463–1474
Bagasra O (1999) HIV and molecular immunity: prospect for AIDS vaccine. Eaton publishing, Natick, MA, USA
Bagasra O, Pace G (2010) A new perspective on HIV vaccine design: a view point. Ibnosina J Med and Biomed Sci 2(1):1–13
Bagasra O, Amjad M (2000) Protection against retroviruses is owing to a different form of immunity: a RNA-based molecular immunity hypothesis. Appl Immunohistochem Mol Morphol 8:133–146
Bagasra O, Amjad M (1997) Natural immunity against HIV-1: prospect for AIDS vaccine. Front Biosci 2:387–402
Bagasra O, Stir AE, Pirisi-Creek L, Creek KE, Bagasra AU, Glenn N, Lee JS (2006) Role of Micro-RNAs in regulation of lentiviral latency and persistence. Appl Immunohistochem Mol Morphol 14:276–290
Bai Y, Casola C, Betrán E (2008) Evolutionary origin of regulatory regions of retrogenes in Drosophila. BMC Genomics 9:240–250
Banfield JF, Young M (2009) Microbiology. Variety – the splice of life – in microbial communities. Science 326:1198–1199
Bartosik D, Sochacka M, Baj J (2003) Identification and characterization of transposable elements of Paracoccus pantotrophus. J Bacteriol 185(13):3753–3763
Brouns SJ, Jore MM, Lundgren M, Westra ER, Slijkhuis RJ, Snijders AP, Dickman MJ, Makarova KS, Koonin EV, van der Oost J (2008) Small CRISPR RNAs guide antiviral defense in prokaryotes. Science 321(5891):922–923
Buchon N, Vaury C (2006) RNAi: a defensive RNA-silencing against viruses and transposable elements. Heredity 96(2):195–202
Burnet FM (1959) The clonal selection theory of acquired immunity. Vanderbilt University Press, TN
Caswell JL, Mallick S, Richter DJ, Neubauer J, Schirmer C, Gnerre S, Reich D (2008) Analysis of chimpanzee history based on genome sequence alignments. PLoS Genetics 4:e10000057
Conley AB, Piriyapongsa J, Jordan IK (2008a) Retroviral promoters in the human genome. Bioinformatics 24:1563–1567
Conley AB, Miller WJ, Jordan IK (2008b) Human cis natural antisense transcripts initiated by transposable elements. Trends Genet 24:53–56
de Kruif P (1926) Microbe hunters. Harcourt, Brace and Company, New York
Doolittle RF, Sapienza C (1980) Selfish genes, the phenotypic paradigm, and genome evolution. Nature 284:601–603
Dooner HK, Weil CF (2007) Give-and-take: interactions between DNA transposons and their host plant genomes. Curr Opin Genet Dev 17:486–492
Dunn CW, Hejnol A, Matus DQ, Pang K, Browne WE, Smith SA, Seaver E, Rouse GW, Obst M, Edgecombe GD, Sørensen MV, Haddock SH, Schmidt-Rhaesa A, Okusu A, Kristensen RM, Wheeler WC, Martindale MQ, Giribet G (2008) Broad phylogenomic sampling improves resolution of the animal tree of life. Nature 452:745–749
Frenkel N, Schirmer EC, Wyatt LS, Katsafanas G, Roffman E, Danovich RM, June CH (1990) Isolation of a new herpesvirus from human CD4+ T cells. Proc Natl Acad Sci USA 87:748–752
Furesz J, Levenbook I (1998) New assays for the quality control of live oral poliovirus vaccine. Acta Microbiol Immunol Hung 45(3–4):391–399
Hakim ST, Alsayari M, McLean DC, Saleem S, Addanki KC, Aggarwal M, Mahalingam K, Bagasra O (2008) A large number of the human microRNAs target lentiviruses, retroviruses, and endogenous retroviruses. BBRC 369:357–362
Han CG, Shiga Y, Tobe T, Sasakawa C, Ohtsubo E (2001) Structural and functional characterization of IS679 and IS66-family elements. J Bacteriol 183:4296–4304
Harris J (2009) Soil microbial communities and restoration ecology: facilitators or followers? Science 325:573–574
Helm T (2004) Basic immunology: a primer. Minn Med 87(5):40–44
Heimberg AM, Sempere LF, Moy VN, Donoghue PC, Peterson KJ (2008) MicroRNAs and the advent of vertebrate morphological complexity. Proc Natl Acad Sci USA 105:2946–2950
Horvath P, Barrangou R (2010) CRISPR/Cas, the immune system of bacteria and archaea. Science 327(5962):167–170
Jordan IK, Rogozin IB, Wolf YI, Koonin EV (2002) Microevolutionary genomics of bacteria. Theor Popul Biol 61(4):435–447
Jordan IK, Rogozin IB, Glazko GV, Koonin EV (2003) Origin of a substantial fraction of human regulatory sequences from transposable elements. Trends Genet 19(2):68–72
Karp CL, Auwaerter PG (2007) Coinfection with HIV and tropical infectious diseases. II. Helminthic, fungal, bacterial and viral pathogens. Clin Infect Dis 45:1214–1220
Karttunen A, Pöyry T, Vaarala O, Ilonen J, Hovi T, Roivainen M, Hyypiä T (2003) Variation in enterovirus receptor genes. J Med Virol 70(1):99–108
Kidwell MG, Lisch DR (2001) Perspective: transposable elements, parasitic DNA, genome evolution. Evolution 55:1–24
Lisch D (2002) Mutator transposons. Trends Plant Sci 7:498–504
Lisco A, Grivel JC, Biancotto A, Vanpouille C, Origgi F, Malnati MS, Schols D, Lusso P, Margolis LB (2007) Viral interactions in human lymphoid tissue: human herpesvirus 7 suppresses the replication of CCR5-tropic human immunodeficiency virus type 1 via CD4 modulation. J Virol 81:708–717
Lusso P, Secchiero P, Crowley RW, Garzino-Demo A, Berneman ZN, Gallo RC (1994) CD4 is a critical component of the receptor for human herpesvirus 7: Interference with human immunodeficiency virus. Proc Natl Acad Sci USA 91:3872–3876
Matzke MA, Mette MF, Matzke AJ (2000) Transgene silencing by the host genome defense: implications for the evolution of epigenetic control mechanisms in plants and vertebrates. Plant Mol Biol 43:401–415
Muotri AR, Marchetto MC, Coufal NG, Gage FH (2007) The necessary junk: new functions for transposable elements. Hum Mol Genet 16(Review Issue 2):R159–R167
Navon R, Wang H, Steinfeld I, Tsalenko A, Ben-Dor A, Yakhini Z (2009) Novel rank-based statistical methods reveal microRNAs with differential expression in multiple cancer types. PLoS One 4(11):e8003
Obbard DJ, Gordon KH, Buck AH, Jiggins FM (2009) The evolution of RNAi as a defence against viruses and transposable elements. Philos Trans R Soc Lond B Biol Sci 364:99–115
Ochman H, Raghavan R (2009) Systems biology. Excavating the functional landscape of bacterial cells. Science 326:1200–1201
Palm NW, Medzhitov R (2009) Pattern recognition receptors and control of adaptive immunity. Immunol Rev 227(1):221–233
Pandrea I, Sodora DL, Silvestri G, Apetrei C (2008) Into the wild: simian immunodeficiency virus (SIV) infection in natural hosts. Trends Immunol 29:419–428
Piriyapongsa J, Jordan IK (2008) Dual coding of siRNAs and miRNAs by plant transposable elements. RNA 14:814–821
Pradeu T (2009) Immune system: “Big Bang” in question. Science 325(5939):393
Ryt-Hansen R, Katzenstein TL, Gerstoft J, Eugen-Olsen J (2006) No influence of GB virus C on disease progression in a Danish cohort of HIV-infected men. AIDS Res Hum Retroviruses 22:496–498
Schluter SF, Marchalonis JJ (2003) Cloning of shark RAG2 and characterization of the RAG1/RAG2 gene locus. FASEB J 17:470–472
Schott DH, Cureton DK, Whelan SP, Hunter CP (2005) An antiviral role for the RNA interference machinery in Caenorhabditis elegans. Proc Natl Acad Sci USA 102:18420–18424
Schmeier S, MacPherson CR, Essack M, Kaur M, Schaefer U, Suzuki H, Hayashizaki Y, Bajic VB (2009) Deciphering the transcriptional circuitry of microRNA genes expressed during human monocytic differentiation. BMC Genomics 10:595
Schramke V, Allshire R (2003) Hairpin RNAs and retrotransposon LTRs effect RNAi and chromatin-based gene silencing. Science 301:1069–1074
Shabalina SA, Koonin EV (2008) Origins and evolution of eukaryotic RNA interference. Trends Ecol Evol 23(10):578–587
Siomi MC, Siomi H (2008) Characterization of endogenous human Argonautes and their miRNA partners in RNA silencing. Nucleic Acids Symp Ser (Oxf) 52:59–60
Sompayrac LM (2008) How the immune system works, 3rd edn. Wiley-Blackwel, Malden, MA
Szathmáry E (1999) The origin of the genetic code: amino acids as cofactors in an RNA world. Trends Genet 15:223–229
Taganov KD, Boldin MP, Baltimore D (2007) MicroRNAs and immunity: tiny players in a big field. Immunity 26:133–137
Tang TH, Polacek N, Zywicki M, Huber H, Brugger K, Garrett R, Bachellerie JP, Hüttenhofer A (2005) Identification of novel non-coding RNAs as potential antisense regulators in the archaeon Sulfolobus solfataricus. Mol Microbiol 55(2):469–481
Thompson CB (1995) New insights into V(D)J recombination and its role in the evolution of the immune system. Immunity 3(5):531–539
Ulenga NK, Sarr AD, Hamel D, Sankale JL, Mboup S, Kanki PJ (2008) The level of APOBEC3G (hA3G)-related G-to-A mutations does not correlate with viral load in HIV type 1-infected individuals. AIDS Res Human Ret 24:1285–1290
Walker BD, Goulder PJ (2000) AIDS. Escape from the immune system. Nature 407:313–314
Zamore PD (2006) RNA interference: big applause for silencing in Stockholm. Cell 127:1083–1086
Acknowledgment
We would like to thank Robert T. Pace for his art work for Figure 1. This work was partially supported by a grant from the US Department of Energy (grant #DE-EM0000479).
Author information
Authors and Affiliations
Corresponding author
Editor information
Editors and Affiliations
Appendix
Appendix
Abbreviation | Term | Meaning |
---|---|---|
Ago | Argonaute protein | The catalytic core of RISC that binds short RNAs and, in many cases, displays RNase H-like mRNA-cleaving activity. Key domains include the PAZ (Piwi-Argonaute-Zwille) and Piwi domains. Ago is named after an Arabidopsis developmental mutant that resembles the tentacles of a paper nautilus (Argonautidae) |
Dcr | Dicer protein | The RNase-III family ribonuclease that cleaves dsRNA into short RNAs. Key domains include a helicase C-terminal domain, dsRNA-binding domains, a PAZ domain and two RNase-III domains. Named for its “dicing” activity |
dsRNA | Double-stranded RNA | Small double-stranded RNAs are the basic molecules involved in gene silencing, gene regulation and viral defense |
endo-siRNA | Endogenous siRNA | A short RNA (other than an miRNA) that is derived from the host genome, rather than an exogenous source (e.g. a virus) |
IS | Insertional sequences | The most basic of transposable element forms, which are part of practically every bacterial genome, are the insertion sequences |
miRNA | microRNA | Single-stranded RNAs of 21–22 nt, derived from short fold-back hairpins (pre-miRNAs) and involved in translational control |
piRNA | Piwi-interacting RNA | Single-stranded RNAs of 24–29 nt that function in complex with Piwi family Argonaute proteins in the animal germ line |
rasiRNA | Repeat-associated siRNA | Short RNAs derived from repeat sequences, such as TEs, sometimes considered a subclass of piRNAs in Drosophila |
RdRp | RNA-dependent RNA polymerase | RNA polymerase directed by RNA, especially eukaryotic polymerases involved in the amplification of RNAi in nematodes and plants |
RISC | RNA-induced silencing complex | The complex comprising Argonaute, a short RNA, and several other proteins, which mediates RNAi through sequence-specific complementarity |
RNAi | RNA interference | The class of processes that use short single-stranded RNA molecules in complex with an Argonaute protein to bind complementary nucleic acids and modify their action and/or processing |
siRNA | Short interfering RNA | Single-stranded RNAs of 20–30 nt involved in RNAi (especially those not classed as microRNAs) |
ncRNA | Small noncoding RNA | Small noncoding RNAs play a crucial role in molecular immunity based on sequence homology |
SRNA | Small nucleolar-like RNA | The pre-RNA that are several hundred to thousand or so bp long and contain hairpin structure. These molecules are cut into smaller size and exported to cytoplasm by Exportin-5. Subsequently they take the shape of siRNA |
TE | Transposable element | A stretch of DNA capable of moving around the genome, either by excision (cut-and-paste transposons) or through an RNA intermediate (retro-elements) |
UTR | Untranslated region | Nonprotein-coding regions at the 5′ and 3′ ends of an mRNA |
viRNA | Viral RNA | siRNAs derived from viral sequences |
VSR | Viral suppressor of RNAi | Any viral gene that inhibits host RNAi function |
Rights and permissions
Copyright information
© 2011 Springer-Verlag Berlin Heidelberg
About this chapter
Cite this chapter
Bagasra, O., Pace, D.G. (2011). Back to the Soil: Retroviruses and Transposons. In: Witzany, G. (eds) Biocommunication in Soil Microorganisms. Soil Biology, vol 23. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-14512-4_6
Download citation
DOI: https://doi.org/10.1007/978-3-642-14512-4_6
Published:
Publisher Name: Springer, Berlin, Heidelberg
Print ISBN: 978-3-642-14511-7
Online ISBN: 978-3-642-14512-4
eBook Packages: Biomedical and Life SciencesBiomedical and Life Sciences (R0)