ATRX-DAXX Complex Expression Levels and Telomere Length in Normal Young and Elder Autopsy Human Brains

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Citações na Scopus
1
Tipo de produção
article
Data de publicação
2019
Título da Revista
ISSN da Revista
Título do Volume
Editora
MARY ANN LIEBERT, INC
Citação
DNA AND CELL BIOLOGY, v.38, n.9, p.955-961, 2019
Projetos de Pesquisa
Unidades Organizacionais
Fascículo
Resumo
The chromatin-remodeling complex ATRX/DAXX is one of the major epigenetic factors that controls heterochromatin maintenance due to its role in histone deposition. ATRX is involved in nucleosome configuration and maintenance of higher order chromatin structure, and DAXX is a specific histone chaperone for H3.3 deposition. Dysfunctions in this complex have been associated with telomere shortening, which influences cell senescence. However, data about this complex in brain tissue related to aging are still scarce. Therefore, in the present study, we analyzed ATRX and DAXX expressions in autopsied human brain specimens and the telomere length. A significant decrease in gene and protein expressions was observed in the brain tissues from the elderly compared with those from the young, which were related to short telomeres. These findings may motivate further functional analysis to confirm the ATRX-DAXX complex involvement in telomere maintenance and brain aging.
Palavras-chave
ATRX, DAXX, gene and protein expressions, human brain tissues, aging, telomere length
Referências
  1. Baumann C, 2010, PLOS GENET, V6, DOI 10.1371/journal.pgen.1001137
  2. Bernadotte A, 2016, AGING-US, V8, P3, DOI 10.18632/aging.100871
  3. Cawthon RM, 2002, NUCLEIC ACIDS RES, V30, DOI 10.1093/nar/30.10.e47
  4. Clynes D, 2015, NAT COMMUN, V6, DOI 10.1038/ncomms8538
  5. Clynes D, 2014, PLOS ONE, V9, DOI 10.1371/journal.pone.0092915
  6. Clynes D, 2013, TRENDS BIOCHEM SCI, V38, P461, DOI 10.1016/j.tibs.2013.06.011
  7. De La Fuente R, 2004, DEV BIOL, V272, P1, DOI 10.1016/j.ydbio.2003.12.012
  8. Drane P, 2010, GENE DEV, V24, P1253, DOI 10.1101/gad.566910
  9. Dyer MA, 2017, CSH PERSPECT MED, V7, DOI 10.1101/cshperspect.a026567
  10. Heaphy CM, 2011, SCIENCE, V333, P425, DOI 10.1126/science.1207313
  11. Hofmann TG, 2003, CANCER RES, V63, P8271
  12. Hollenbach AD, 2002, J CELL SCI, V115, P3319
  13. Kovatcheva M, 2017, NAT COMMUN, V8, DOI 10.1038/s41467-017-00540-5
  14. Langst G, 2015, GENES-BASEL, V6, P299, DOI 10.3390/genes6020299
  15. Law MJ, 2010, CELL, V143, P367, DOI 10.1016/j.cell.2010.09.023
  16. Lessard-Beaudoin M, 2016, BIOGERONTOLOGY, V17, P817, DOI 10.1007/s10522-016-9651-y
  17. Lewis PW, 2010, P NATL ACAD SCI USA, V107, P14075, DOI 10.1073/pnas.1008850107
  18. Liau JY, 2015, HUM PATHOL, V46, P1360, DOI 10.1016/j.humpath.2015.05.019
  19. Michod D, 2012, NEURON, V74, P122, DOI 10.1016/j.neuron.2012.02.021
  20. Muromoto R, 2004, J IMMUNOL, V172, P2985, DOI 10.4049/jimmunol.172.5.2985
  21. Napier CE, 2015, ONCOTARGET, V6, P16543, DOI 10.18632/oncotarget.3846
  22. Neidle S, 2003, CURR OPIN STRUC BIOL, V13, P275, DOI 10.1016/S0959-440X(03)00072-1
  23. Piazzesi A, 2016, CELL REP, V17, P987, DOI 10.1016/j.celrep.2016.09.074
  24. Ritchie K, 2008, J CELL BIOL, V180, P315, DOI 10.1083/jcb.200706083
  25. Salomoni P, 2013, FRONT ONCOL, V3, DOI 10.3389/fonc.2013.00152
  26. Saretzki Gabriele, 2018, Subcell Biochem, V90, P221, DOI 10.1007/978-981-13-2835-0_9
  27. Schindelin J, 2012, NAT METHODS, V9, P676, DOI [10.1038/NMETH.2019, 10.1038/nmeth.2019]
  28. Schmittgen TD, 2008, NAT PROTOC, V3, P1101, DOI 10.1038/nprot.2008.73
  29. Schwartzentruber J, 2012, NATURE, V482, P226, DOI 10.1038/nature10833
  30. Seah C, 2008, J NEUROSCI, V28, P12570, DOI 10.1523/JNEUROSCI.4048-08.2008
  31. Vandesompele J, 2002, GENOME BIOL, V3, DOI 10.1186/gb-2002-3-7-research0034
  32. Victorelli S, 2017, EBIOMEDICINE, V21, P14, DOI 10.1016/j.ebiom.2017.03.027
  33. Watson LA, 2013, J CLIN INVEST, V123, P2049, DOI 10.1172/JCI65634
  34. Wong LH, 2010, GENOME RES, V20, P351, DOI 10.1101/gr.101477.109
  35. World Health Organization, 2015, WORLD REP AG HLTH
  36. Wysoczanska B, 2013, POSTEP HIG MED DOSW, V67, P1319, DOI 10.5604/17322693.1081034