Genome-wide analysis reveals no evidence of trans chromosomal regulation of mammalian immune development

被引:17
作者
Johanson, Timothy M. [1 ,2 ]
Coughlan, Hannah D. [1 ,2 ]
Lun, Aaron T. L. [1 ,2 ]
Bediaga, Naiara G. [1 ,2 ]
Naselli, Gaetano [1 ]
Garnham, Alexandra L. [1 ,2 ]
Harrison, Leonard C. [1 ,2 ]
Smyth, Gordon K. [1 ,3 ]
Allan, Rhys S. [1 ,2 ]
机构
[1] Walter & Eliza Hall Inst Med Res, Parkville, Vic, Australia
[2] Univ Melbourne, Dept Med Biol, Parkville, Vic, Australia
[3] Univ Melbourne, Sch Math & Stat, Parkville, Vic, Australia
来源
PLOS GENETICS | 2018年 / 14卷 / 06期
基金
英国医学研究理事会; 澳大利亚研究理事会;
关键词
INTERCHROMOSOMAL ASSOCIATIONS; X-INACTIVATION; EXPRESSION; ENHANCER; GENE; COLOCALIZATION; ARCHITECTURE; MAINTENANCE; PRINCIPLES; CTCF;
D O I
10.1371/journal.pgen.1007431
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
It has been proposed that interactions between mammalian chromosomes, or transchromosomal interactions (also known as kissing chromosomes), regulate gene expression and cell fate determination. Here we aimed to identify novel transchromosomal interactions in immune cells by high-resolution genome-wide chromosome conformation capture. Although we readily identified stable interactions in cis, and also between centromeres and telomeres on different chromosomes, surprisingly we identified no gene regulatory transchromosomal interactions in either mouse or human cells, including previously described interactions. We suggest that advances in the chromosome conformation capture technique and the unbiased nature of this approach allow more reliable capture of interactions between chromosomes than previous methods. Overall our findings suggest that stable transchromosomal interactions that regulate gene expression are not present in mammalian immune cells and that lineage identity is governed by cis, not trans chromosomal interactions.
引用
收藏
页数:14
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