Positive selection drives the evolution of rhino, a member of the heterochromatin protein 1 family in Drosophila.

作者: Danielle Vermaak , Steven Henikoff , Harmit S Malik

DOI: 10.1371/JOURNAL.PGEN.0010009

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摘要: Heterochromatin comprises a significant component of many eukaryotic genomes. In comparison to euchromatin, heterochromatin is gene poor, transposon rich, and late replicating. It serves important biological roles, from silencing accurate chromosome segregation, yet little known about the evolutionary constraints that shape heterochromatin. A complementary approach traditional one directly studying heterochromatic DNA sequence study evolution proteins bind define One best markers for protein 1 (HP1), which an essential, nonhistone chromosomal protein. Here we investigate molecular five HP1 paralogs present in Drosophila melanogaster. Three these have ubiquitous expression patterns adult tissues, whereas HP1D/rhino HP1E are expressed predominantly ovaries testes respectively. The also distinct localization preferences cells. Thus, Rhino localizes compartment tissue culture cells, but pattern HP1A lysine-9 dimethylated H3. Using population genetic analyses, find rhino has been subject positive selection all three domains protein: N-terminal chromo domain, C-terminal chromo-shadow hinge region connects two modules. Maximum likelihood analysis sequences 20 species reveals small number residues shadow repeated selection. rapid highly unusual encoding suggests involved conflict affects germline, belying notion simply passive recipient “junk DNA”

参考文章(85)
E. Minc, Y. Allory, J.-C. Courvalin, Brigitte Buendia, Immunolocalization of HP1 proteins in metaphasic mammalian chromosomes Chromosome Painting. ,vol. 23, pp. 171- 174 ,(2001) , 10.1007/978-94-010-0330-8_18
Mohammed M. Shareef, RamaKrishna Badugu, Rebecca Kellum, HP1/ORC complex and heterochromatin assembly. Genetica. ,vol. 117, pp. 127- 134 ,(2003) , 10.1023/A:1022963223220
J. S. Platero, T. Hartnett, J. C. Eissenberg, Functional analysis of the chromo domain of HP1. The EMBO Journal. ,vol. 14, pp. 3977- 3986 ,(1995) , 10.1002/J.1460-2075.1995.TB00069.X
Andrew J. Bannister, Philip Zegerman, Janet F. Partridge, Eric A. Miska, Jean O. Thomas, Robin C. Allshire, Tony Kouzarides, Selective recognition of methylated lysine 9 on histone H3 by the HP1 chromo domain. Nature. ,vol. 410, pp. 120- 124 ,(2001) , 10.1038/35065138
Bas van Steensel, Steven Henikoff, Identification of in vivo DNA targets of chromatin proteins using tethered dam methyltransferase. Nature Biotechnology. ,vol. 18, pp. 424- 428 ,(2000) , 10.1038/74487
Monika Lachner, Dónal O'Carroll, Stephen Rea, Karl Mechtler, Thomas Jenuwein, Methylation of histone H3 lysine 9 creates a binding site for HP1 proteins. Nature. ,vol. 410, pp. 116- 120 ,(2001) , 10.1038/35065132
K R Peterson, M G Kidwell, A Chovnick, S B Daniels, L D Strausbaugh, Evidence for horizontal transmission of the P transposable element between Drosophila species. Genetics. ,vol. 124, pp. 339- 355 ,(1990) , 10.1093/GENETICS/124.2.339
Paul B Talbert, Terri D Bryson, Steven Henikoff, Adaptive evolution of centromere proteins in plants and animals Journal of Biology. ,vol. 3, pp. 18- 18 ,(2004) , 10.1186/JBIOL11