Pai et al.
(2011) |
Human, chimpanzee |
Heart, liver, kidney |
Illumina 27K Chip |
Substantial inter-tissue conservation across species. 12–18%
of interspecies differences in expression are associated
with promoter methylation differences |
Molaro et
al. (2011) |
Human, chimpanzee |
Sperm |
WGBS |
Average correlation between the two species is 0.87 |
Reported that human-specific hypo-methylated regions occur
near genes encoding neurological functions |
Martin et al.
(2011) |
Human, chimpanzee, orangutan |
Neutrophils |
HpaII digestion and MethylSeq |
High conservation methylome-wide except for ∼10% CpG
island-like regions |
Hodges et al.
(2011) |
Human, chimpanzee |
HSPC, B cells, neutrophils |
WGBS |
Hypo-methylated regions show significant overlap between
species. Inter-tissue variability of region-length is
similar in humans and chimpanzees |
Zeng et al.
(2012) |
Human, chimpanzee |
Prefrontal cortex |
WGBS |
3.5% (474/13,454) promoters are differentially
methylated |
Wang et
al. (2012) |
Human, macaque |
Prefrontal cortex |
MeDIP-Chip and SEQUENOM MassARRAY |
Patterns of methylation of the brain are similar, with only
few differentially methylated regions identified. |
Identified two differentially methylated regions with
protein-conservation involved in neural functions |
Hernando-Herraez et
al. (2013) |
Human, chimpanzee, bonobo, gorilla, orangutan |
Peripheral blood |
Illumina 450K Chip |
Correspondence between protein sequence and gene regulation
except for ∼800 genes.184 genes perfectly conserved at
protein level show epigenetic differences between humans and
chimpanzees |