Chromatin conformation and histone modification profiling across human kidney anatomic regions
被引:0
|
作者:
Li, Haikuo
论文数: 0引用数: 0
h-index: 0
机构:
Washington Univ St Louis, Dept Med, Div Nephrol, St Louis, MO 63130 USAWashington Univ St Louis, Dept Med, Div Nephrol, St Louis, MO 63130 USA
Li, Haikuo
[1
]
Li, Dian
论文数: 0引用数: 0
h-index: 0
机构:
Washington Univ St Louis, Dept Med, Div Nephrol, St Louis, MO 63130 USAWashington Univ St Louis, Dept Med, Div Nephrol, St Louis, MO 63130 USA
Li, Dian
[1
]
Humphreys, Benjamin D.
论文数: 0引用数: 0
h-index: 0
机构:
Washington Univ St Louis, Dept Med, Div Nephrol, St Louis, MO 63130 USA
Washington Univ St Louis, Dept Dev Biol, St Louis, MO 63130 USAWashington Univ St Louis, Dept Med, Div Nephrol, St Louis, MO 63130 USA
Humphreys, Benjamin D.
[1
,2
]
机构:
[1] Washington Univ St Louis, Dept Med, Div Nephrol, St Louis, MO 63130 USA
[2] Washington Univ St Louis, Dept Dev Biol, St Louis, MO 63130 USA
The three major anatomic regions of the human kidney include the cortex, medulla and papilla, with different functions and vulnerabilities to kidney diseases. Epigenetic mechanisms underlying these anatomic structures are incompletely understood. Here, we performed chromatin conformation capture with Hi-C and histone modification H3K4me3/H3K27me3 Cleavage Under Targets and Release Using Nuclease (CUT&RUN) sequencing on the kidney cortex, medulla and papilla dissected from one individual donor. Nuclear suspensions were generated from each region and split subjected to paired Hi-C and CUT&RUN sequencing. We evaluated the quality of next-generation sequencing data, Hi-C chromatin contact matrices and CUT&RUN peak calling. H3K4me3 and H3K27me3 histone modifications represent active and repressive gene transcription, respectively, and differences in chromatin conformation between kidney regions can be analyzed with this dataset. All raw and processed data files are publicly available, allowing researchers to survey the epigenetic landscape across regional human kidney anatomy.