Результаты исследований: Научные публикации в периодических изданиях › статья › Рецензирование
The evolution of CpG islands by tandem duplications. / Babenko, V. N.; Orlov, Yu L.; Isakova, Zh T. и др.
в: Russian Journal of Genetics: Applied Research, Том 7, № 5, 01.07.2017, стр. 538-549.Результаты исследований: Научные публикации в периодических изданиях › статья › Рецензирование
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TY - JOUR
T1 - The evolution of CpG islands by tandem duplications
AU - Babenko, V. N.
AU - Orlov, Yu L.
AU - Isakova, Zh T.
AU - Antonov, D. A.
AU - Voevoda, M. I.
N1 - Publisher Copyright: © 2017, Pleiades Publishing, Ltd.
PY - 2017/7/1
Y1 - 2017/7/1
N2 - CG-rich islands (CpG islands or CGI) are important functional elements in the genome of vertebrates. In particular, they (a) initiate transcription—bidirectional in some cases, due to the self-complementarity of the CG dinucleotides—as promoters in most (>50%) genes of vertebrates; (b) form a global methylation landscape; and (c) act to “switch-off” transcription via methylation. The degenerate nature of CpG islands (elevated CG content) implies an increase in the probability of tandem repeats and palindromes within a CpG island. In this work, tandem duplications of complete CpG islands (megamonomers with a length of 400–5000 bp) are identified in the human genome. We have found both intergenic and intragenic tandem duplications of CpG islands. The discovered CGI duplications are mediated through CG-rich subcentromeric and telomeric satellites and SINEs. The similarity of the monomers in tandem repeats in some cases suggests the existence of selection pressure on the structure of such loci. The context of intergenic tandem CGI repeats indicates their potential role in leveling the CG composition in the genome segment. The found tandem CGIs are transcriptionally active in a wide range of tissues and cell lines. The considered phenomenon of CGI cluster organization is most pronounced in chromosome 19, known for abundant segment duplications and gene expansions. The DXZ4 megasatellite, which resides in the long (q) arm of chromosome X, also belonging to the CGIs generated by tandem duplications, is another unique genome segment.
AB - CG-rich islands (CpG islands or CGI) are important functional elements in the genome of vertebrates. In particular, they (a) initiate transcription—bidirectional in some cases, due to the self-complementarity of the CG dinucleotides—as promoters in most (>50%) genes of vertebrates; (b) form a global methylation landscape; and (c) act to “switch-off” transcription via methylation. The degenerate nature of CpG islands (elevated CG content) implies an increase in the probability of tandem repeats and palindromes within a CpG island. In this work, tandem duplications of complete CpG islands (megamonomers with a length of 400–5000 bp) are identified in the human genome. We have found both intergenic and intragenic tandem duplications of CpG islands. The discovered CGI duplications are mediated through CG-rich subcentromeric and telomeric satellites and SINEs. The similarity of the monomers in tandem repeats in some cases suggests the existence of selection pressure on the structure of such loci. The context of intergenic tandem CGI repeats indicates their potential role in leveling the CG composition in the genome segment. The found tandem CGIs are transcriptionally active in a wide range of tissues and cell lines. The considered phenomenon of CGI cluster organization is most pronounced in chromosome 19, known for abundant segment duplications and gene expansions. The DXZ4 megasatellite, which resides in the long (q) arm of chromosome X, also belonging to the CGIs generated by tandem duplications, is another unique genome segment.
KW - chromosome 19
KW - CpG island clusters
KW - CpG islands
KW - epigenetics
KW - GC composition
KW - gene duplications
KW - human genome
KW - macrosatellites
KW - methylation
KW - tandem repeats
UR - http://www.scopus.com/inward/record.url?scp=85028020333&partnerID=8YFLogxK
U2 - 10.1134/S2079059717050033
DO - 10.1134/S2079059717050033
M3 - Article
AN - SCOPUS:85028020333
VL - 7
SP - 538
EP - 549
JO - Russian Journal of Genetics: Applied Research
JF - Russian Journal of Genetics: Applied Research
SN - 2079-0597
IS - 5
ER -
ID: 8966368