Derivation of consensus inactivation status for X-linked genes from genome-wide studies

被引:154
作者
Balaton, Bradley P. [1 ]
Cotton, Allison M. [2 ]
Brown, Carolyn J. [1 ]
机构
[1] Univ British Columbia, Dept Med Genet, Mol Epigenet Grp, Inst Life Sci, Vancouver, BC, Canada
[2] Univ British Columbia, Dept Med Genet, Ctr Mol Med & Therapeut, Child & Family Res Inst, Vancouver, BC, Canada
关键词
X-chromosome inactivation; Dosage compensation; Escape from X-chromosome inactivation; Somatic cell hybrids; Allelic imbalance; DNA methylation; HUMAN CELL-LINES; CHROMOSOME INACTIVATION; DNA METHYLATION; SEX-DIFFERENCES; NONCODING RNA; EXPRESSION; IDENTIFICATION; COMPENSATION; CHROMATIN; TISSUES;
D O I
10.1186/s13293-015-0053-7
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: X chromosome inactivation is the epigenetic silencing of the majority of the genes on one of the X chromosomes in XX therian mammals. In humans, approximately 15 % of genes consistently escape from this inactivation and another 15 % of genes vary between individuals or tissues in whether they are subject to, or escape from, inactivation. Multiple studies have provided inactivation status calls for a large subset of the genes on the X chromosome; however, these studies vary in which genes they were able to make calls for and in some cases which call they give a specific gene. Methods: This analysis aggregated three published studies that have examined X chromosome inactivation status of genes across the X chromosome, generating consensus calls and identifying discordancies. The impact of expression level and chromosomal location on X chromosome inactivation status was also assessed. Results: Overall, we assigned a consensus XCI status 639 genes, including 78 % of protein-coding genes expressed outside of the testes, with a lower frequency for non-coding RNA and testis-specific genes. Study-specific discordancies suggest that there may be instability of XCI during cell culture and also highlight study-specific variations in call type. We observe an enrichment of discordant genes at boundaries between genes subject to and escaping from inactivation. Conclusions: This study has compiled a comprehensive list of X-chromosome inactivation statuses for genes and also discovered some biases which will help guide future studies examining X-chromosome inactivation.
引用
收藏
页数:11
相关论文
共 53 条
[1]   CTdatabase: a knowledge-base of high-throughput and curated data on cancer-testis antigens [J].
Almeida, Luiz Gonzaga ;
Sakabe, Noboru J. ;
deOliveira, Alice R. ;
Silva, Maria Cristina C. ;
Mundstein, Alex S. ;
Cohen, Tzeela ;
Chen, Yao-Tseng ;
Chua, Ramon ;
Gurung, Sita ;
Gnjatic, Sacha ;
Jungbluth, Achim A. ;
Caballero, Otavia L. ;
Bairoch, Amos ;
Kiesler, Eva ;
White, Sarah L. ;
Simpson, Andrew J. G. ;
Old, Lloyd J. ;
Camargo, Anamaria A. ;
Vasconcelos, Ana Tereza R. .
NUCLEIC ACIDS RESEARCH, 2009, 37 :D816-D819
[2]  
[Anonymous], 2022, Modern Applied Statistics with S
[3]  
[Anonymous], PROG CLIN BIOL RES
[4]   Identification of sexually dimorphic genes in the neonatal mouse cortex and hippocampus [J].
Armoskus, Chris ;
Moreira, Debbie ;
Bollinger, Kayla ;
Jimenez, Oliva ;
Taniguchi, Saori ;
Tsai, Houng-Wei .
BRAIN RESEARCH, 2014, 1562 :23-38
[5]   Conceptual frameworks and mouse models for studying sex differences in physiology and disease: Why compensation changes the game [J].
Arnold, Arthur P. .
EXPERIMENTAL NEUROLOGY, 2014, 259 :2-9
[6]  
Bennett-Baker PE, 2003, GENETICS, V165, P2055
[7]   Escape from X Inactivation Varies in Mouse Tissues [J].
Berletch, Joel B. ;
Ma, Wenxiu ;
Yang, Fan ;
Shendure, Jay ;
Noble, William S. ;
Disteche, Christine M. ;
Deng, Xinxian .
PLOS GENETICS, 2015, 11 (03)
[8]   Mutations in DDX3X Are a Common Cause of Unexplained Intellectual Disability with Gender-Specific Effects on Wnt Signaling [J].
Blok, Lot Snijders ;
Madsen, Erik ;
Juusola, Jane ;
Gilissen, Christian ;
Baralle, Diana ;
Reijnders, Margot R. F. ;
Venselaar, Hanka ;
Helsmoorte, Celine ;
Cho, Megan T. ;
Hoischen, Alexander ;
Vissers, Lisenka E. L. M. ;
Koemans, Tom S. ;
Wissink-Lindhout, Willemijn ;
Eichler, Evan E. ;
Romano, Corrado ;
Van Esch, Hilde ;
Stumpel, Connie ;
Vreeburg, Maaike ;
Smeets, Eric ;
Obemdorff, Karin ;
van Bon, Bregje W. M. ;
Shaw, Marie ;
Gecz, Jozef ;
Haan, Eric ;
Bienek, Melanie ;
Jensen, Corinna ;
Loeys, Bart L. ;
Van Diick, Anke ;
Innes, A. Micheil ;
Racher, Hilary ;
Vermeer, Sascha ;
Di Donato, Nataliya ;
Rump, Andreas ;
Tatton-Brown, Katrina ;
Parker, Michael J. ;
Henderson, Alex ;
Lynch, Sally A. ;
Fryer, Alan ;
Ross, Alison ;
Vasudevan, Pradeep ;
Kini, Usha ;
Newbury-Ecob, Ruth ;
Chandler, Kate ;
Male, Alison ;
Dijkstra, Sybe ;
Schieving, Jolanda ;
Giltay, Jacques ;
Van Gassen, Koen L. I. ;
Schuurs-Hoeijmakers, Janneke ;
Tan, Perciliz L. .
AMERICAN JOURNAL OF HUMAN GENETICS, 2015, 97 (02) :343-352
[9]   Gene: a gene-centered information resource at NCBI [J].
Brown, Garth R. ;
Hem, Vichet ;
Katz, Kenneth S. ;
Ovetsky, Michael ;
Wallin, Craig ;
Ermolaeva, Olga ;
Tolstoy, Igor ;
Tatusova, Tatiana ;
Pruitt, Kim D. ;
Maglott, Donna R. ;
Murphy, Terence D. .
NUCLEIC ACIDS RESEARCH, 2015, 43 (D1) :D36-D42
[10]   X-inactivation profile reveals extensive variability in X-linked gene expression in females [J].
Carrel, L ;
Willard, HF .
NATURE, 2005, 434 (7031) :400-404