Public Service by a Selfish Gene: A Domesticated Transposase Antagonizes Polycomb Function


Published in the journal: . PLoS Genet 12(6): e32767. doi:10.1371/journal.pgen.1006014
Category: Perspective
doi: 10.1371/journal.pgen.1006014

Summary

article has not abstract

Eukaryotic genomes are littered with transposable elements (TEs)—“selfish” genetic entities capable of increasing copy numbers through transposition to account for large fractions of the nuclear DNA. To minimize the mutagenic effects of transposition, host organisms have evolved various mechanisms to repress TE-encoded genes (TEGs) both transcriptionally through chromatin modifications and post-transcriptionally through RNA interference. Over time, silenced TEs accumulate genetic mutations, become immobilized, and are eliminated from the genome by recombination or decay into intergenic DNA. But can immobilized TEGs fortuitously acquire cellular functions that are beneficial to the host and become a useful fixture of the genome? In a recent issue of PLOS Genetics, Turck, Goodrich, and colleagues describe a clear example of this process, in which a transposase-derived gene functions to antagonize transcriptional repression by the Polycomb group (PcG) genes in Arabidopsis thaliana [1].

PcG genes play critically important roles in regulating plant development by targeting thousands of genes for transcriptional repression through trimethylation of lysine 27 on histone H3 (H3K27me3) [2]. In Arabidopsis, PcG function requires two classes of protein complexes: Polycomb Repressive Complexes 1 and 2 (PRC1 and PRC2, respectively). The enzymatic complex PRC2 contains one of the three H3K27 trimethyltransferases, MEDEA (MEA), CURLY LEAF (CLF), and SWINGER (SWN), whereas the PRC1 complex includes the H3K27me3-binding protein LIKE HETEROCHROMATIN PROTEIN 1 (LHP1). To better understand the mechanisms that may counteract PcG repression, two independent suppressor screens were performed to identify mutants that could revert the developmental and transcriptional defects of the CLF and LHP1 mutants, respectively [1,3]. One gene named ANTAGONIST OF LIKE HETEROCHROMATIN PROTEIN 1 (ALP1) was isolated from both screens, indicating that it likely functions broadly in antagonizing PcG repression [1,3]. This notion is supported by several lines of evidence: (1) alp1 suppresses the developmental phenotypes of clf; (2) a significant faction of genes overexpressed in clf are no longer overexpressed in alp1 clf; (3) ALP1 functions upstream of PcG-repressed genes (e.g., AGAMOUS); (4) many PcG-target genes are down-regulated in alp1 when normal PcG activity is present; (5) alp1 enhances the defects of several mutants of trithorax group (trxG) genes involved in counteracting PcG repression; and (6) ALP1 physically interacts with PRC2 in planta. Taken together, these results strongly indicate that ALP1 is generally required to antagonize PcG repression at a large number of developmentally important genes [1].

Interestingly, ALP1 encodes a protein that is highly similar to the transposases (TPases) of the PIF/Harbinger superfamily of DNA TEs [1,3]. The first active member of the superfamily, P Instability Factor (PIF), was identified in maize as repeated mutagenic insertions into the anthocyanin regulatory gene R and was later found to be similar to the Harbinger elements computationally identified from Arabidopsis [46]. The PIF/Harbinger superfamily is distantly related to the bacterial IS5 elements and includes five major groups in eukaryotes: two separate plant-specific groups (PIF- and Pong-like groups), an animal-specific group, and two fungal groups [7]. Members of the PIF/Harbinger superfamily share several characteristics: they have short terminal inverted repeats (TIRs), prefer to insert into 3-bp target sites embedded in longer palindromic sequences, and encode two proteins (a Myb-like DNA-binding protein and a TPase) that are both required for transposition [8,9]. ALP1 shares extensive homology with PIF-like TPases. However, there are several important differences: (1) PIF- and Pong-like elements are present at moderate-to-high copy numbers in plant genomes (from dozens in Arabidopsis to ~1,000 in Brassica oleracea), whereas ALP1-like genes are present at single copy in land plants; (2) the DDE catalytic motif in PIF-like TPases is mutated in ALP1 and its homologues in angiosperms (but not in gymnosperms, ferns, bryophtyes, and green algae) and the Myb-like gene and TIRs are missing from ALP1 flanking sequences; and (3) the majority of PIF-like elements are transcriptionally silent and have accumulated missense or nonsense mutations, whereas ALP1 is broadly expressed in Arabidopsis leaves, stems, flowers, and roots, and its coding capacity is well preserved in land plants [1]. Taken together, these results suggest that ALP1 likely originated from a PIF-like TPase gene and acquired an important cellular function in the common ancestor of angiosperms.

In addition to ALP1, a number of TPase-derived genes have been described in eukaryotes (for excellent recent reviews, see [10,11]). The majority of such genes were computationally identified based on the set of characteristics that distinguish ALP1 from PIF TPases, including loss of catalytic activity for transposition, high degree of evolutionary conservation, being present at low copy number, and evidence for transcriptional activity. Importantly, several TPase-derived genes have been shown to provide vital functions for the hosts. For example, the SETMAR protein—created from a fusion between a Mariner TPase and a SET histone methyltransferase domain—is required for the maintenance of genome integrity in primates [12,13]. In plants, the Arabidopsis DAYSLEEPER gene encodes a DNA-binding protein derived from a TPase of the hAT superfamily. DAYSLEEPER binds to a cis-regulatory motif upstream of multiple genes and the daysleeper mutant displays severe and pleiotropic developmental phenotypes [14]. As another example, FHY3 and FAR1 are derived from the MURA TPase gene encoded by Mutator-like elements (MULEs) [15]. However, both FHY3 and FAR1 function as transcription factors that activate gene expression under far-red light.

How ALP1 antagonizes PcG repression and how a TPase acquired such a function remain open questions. Based on the observation that the interactions of PRC1 and ALP1 with PRC2 appeared to be mutually exclusive, Liang et al. proposed that ALP1 may compete with PRC1 for binding to PRC2 and thereby alleviate PcG repression [1]. In this regard, it is interesting to note that, during PIF transposition, the TPase is recruited to TEs by interacting with the Myb-domain protein, which in turn binds specific DNA sequences at TE ends [9]. It is therefore possible that a catalytically inactive mutant TPase with altered preference for protein–protein interactions might have fortuitously acquired PRC2-binding activity. It is also possible that, considering the role of PcG as a “backup system” to repress TE activity (behind DNA methylation) [16], the interaction of a TPase with PRC2 may have originally evolved as an anti-repression mechanism by the TE. Future work should address these questions, for example, by determining whether the same domain is involved in ALP1–PRC2 and TPase–Myb-protein interactions. With the rapid advances of genomic resources and reverse-genetic tools, ALP1 should serve as harbinger of the identification and functional characterization of many more selfish genes that have evolved to serve their hosts.


Zdroje

1. Liang SC, Hartwig B, Perera P, Mora-Garcia S, de Leau E, Thornton H, et al. Kicking against the PRCs—A Domesticated Transposase Antagonises Silencing Mediated by Polycomb Group Proteins and Is an Accessory Component of Polycomb Repressive Complex 2. PLoS Genet. 2015;11(12):e1005660. doi: 10.1371/journal.pgen.1005660 26642436

2. Zhang X, Clarenz O, Cokus S, Bernatavichute YV, Pellegrini M, Goodrich J, et al. Whole-genome analysis of histone H3 lysine 27 trimethylation in Arabidopsis. PLoS Biol. 2007;5(5):e129. 17439305

3. Hartwig B, James GV, Konrad K, Schneeberger K, Turck F. Fast isogenic mapping-by-sequencing of ethyl methanesulfonate-induced mutant bulks. Plant physiology. 2012;160(2):591–600. doi: 10.1104/pp.112.200311 22837357

4. Walker EL, Eggleston WB, Demopulos D, Kermicle J, Dellaporta SL. Insertions of a novel class of transposable elements with a strong target site preference at the r locus of maize. Genetics. 1997;146(2):681–93. 9178016

5. Zhang X, Feschotte C, Zhang Q, Jiang N, Eggleston WB, Wessler SR. P instability factor: an active maize transposon system associated with the amplification of Tourist-like MITEs and a new superfamily of transposases. Proceedings of the National Academy of Sciences of the United States of America. 2001;98(22):12572–7. 11675493

6. Kapitonov VV, Jurka J. Molecular paleontology of transposable elements from Arabidopsis thaliana. Genetica. 1999;107(1–3):27–37. 10952195

7. Zhang X, Jiang N, Feschotte C, Wessler SR. PIF- and Pong-like transposable elements: distribution, evolution and relationship with Tourist-like miniature inverted-repeat transposable elements. Genetics. 2004;166(2):971–86. 15020481

8. Yang G, Zhang F, Hancock CN, Wessler SR. Transposition of the rice miniature inverted repeat transposable element mPing in Arabidopsis thaliana. Proceedings of the National Academy of Sciences of the United States of America. 2007;104(26):10962–7. 17578919

9. Sinzelle L, Kapitonov VV, Grzela DP, Jursch T, Jurka J, Izsvak Z, et al. Transposition of a reconstructed Harbinger element in human cells and functional homology with two transposon-derived cellular genes. Proceedings of the National Academy of Sciences of the United States of America. 2008;105(12):4715–20. doi: 10.1073/pnas.0707746105 18339812

10. Sinzelle L, Izsvak Z, Ivics Z. Molecular domestication of transposable elements: from detrimental parasites to useful host genes. Cellular and molecular life sciences: CMLS. 2009;66(6):1073–93. doi: 10.1007/s00018-009-8376-3 19132291

11. Feschotte C, Pritham EJ. DNA transposons and the evolution of eukaryotic genomes. Annual review of genetics. 2007;41:331–68. 18076328

12. Cordaux R, Udit S, Batzer MA, Feschotte C. Birth of a chimeric primate gene by capture of the transposase gene from a mobile element. Proceedings of the National Academy of Sciences of the United States of America. 2006;103(21):8101–6. 16672366

13. Hromas R, Wray J, Lee SH, Martinez L, Farrington J, Corwin LK, et al. The human set and transposase domain protein Metnase interacts with DNA Ligase IV and enhances the efficiency and accuracy of non-homologous end-joining. DNA repair. 2008;7(12):1927–37. doi: 10.1016/j.dnarep.2008.08.002 18773976

14. Bundock P, Hooykaas P. An Arabidopsis hAT-like transposase is essential for plant development. Nature. 2005;436(7048):282–4. 16015335

15. Lin R, Ding L, Casola C, Ripoll DR, Feschotte C, Wang H. Transposase-derived transcription factors regulate light signaling in Arabidopsis. Science. 2007;318(5854):1302–5. 18033885

16. Deleris A, Stroud H, Bernatavichute Y, Johnson E, Klein G, Schubert D, et al. Loss of the DNA methyltransferase MET1 Induces H3K9 hypermethylation at PcG target genes and redistribution of H3K27 trimethylation to transposons in Arabidopsis thaliana. PLoS Genet. 2012;8(11):e1003062. doi: 10.1371/journal.pgen.1003062 23209430

Štítky
Genetika Reprodukční medicína
Kurzy Doporučená témata Časopisy
Přihlášení
Zapomenuté heslo

Nemáte účet?  Registrujte se

Zapomenuté heslo

Zadejte e-mailovou adresu se kterou jste vytvářel(a) účet, budou Vám na ni zaslány informace k nastavení nového hesla.

Přihlášení

Nemáte účet?  Registrujte se