Schlachetzki, Johannes CM Gianella, Sara Ouyang, Zhengyu Lana, Addison J Yang, Xiaoxu O’Brien, Sydney Challacombe, Jean F Gaskill, Peter J Jordan-Sciutto, Kelly L Chaillon, Antoine
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The presence of HIV in sequestered reservoirs is a central impediment to a functional cure, allowing HIV to persist despite life-long antiretroviral therapy (ART), and driving a variety of comorbid conditions. Our understanding of the latent HIV reservoir in the central nervous system is incomplete, because of difficulties in accessing human centra...
Daly, Adrian Dunnington, Leslie A Rodriguez-Buritica, David F Spiegel, Erica Brancati, Francesco Mantovani, Giovanna Rawal, Vandana M Faucz, Fabio Rueda Hijazi, Hadia CABERG, Jean-Hubert
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peer reviewed / [en] BACKGROUND: X-linked acrogigantism (X-LAG; MIM: 300942) is a severe form of pituitary gigantism caused by chromosome Xq26.3 duplications involving GPR101. X-LAG-associated duplications disrupt the integrity of the topologically associating domain (TAD) containing GPR101 and lead to the formation of a neo-TAD that drives pituita...
Francia, Marcelo Bot, Merel Boltz, Toni De la Hoz, Juan Boks, Marco Kahn, René Ophoff, Roel
Bipolar disorder (BD) is a heritable disorder characterized by shifts in mood that manifest in manic or depressive episodes. Clinical studies have identified abnormalities of the circadian system in BD patients as a hallmark of underlying pathophysiology. Fibroblasts are a well-established in vitro model for measuring circadian patterns. We set out...
Gong, Ting McNally, Karen L Konanoor, Siri Peraza, Alma Bailey, Cynthia Redemann, Stefanie McNally, Francis J
In many animal species, the oocyte meiotic spindle, which is required for chromosome segregation, forms without centrosomes. In some systems, Ran-GEF on chromatin initiates spindle assembly. We found that in Caenorhabditis elegans oocytes, endogenously-tagged Ran-GEF dissociates from chromatin during spindle assembly but re-associates during meioti...
Boulay, Gaylor Broye, Liliane Dong, Rui Iyer, Sowmya Sanalkumar, Rajendran Xing, Yu-Hang Buisson, Rémi Rengarajan, Shruthi Naigles, Beverly Duc, Benoît
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EWS fusion oncoproteins underlie several human malignancies including Desmoplastic Small Round Cell Tumor (DSRCT), an aggressive cancer driven by EWS-WT1 fusion proteins. Here we combine chromatin occupancy and 3D profiles to identify EWS-WT1-dependent gene regulation networks and target genes. We show that EWS-WT1 is a powerful chromatin activator...
Flynn, Sean M Dhir, Somdutta Herka, Krzysztof Doyle, Colm Melidis, Larry Simeone, Angela Hui, Winnie WI Araujo Tavares, Rafael de Cesaris Schoenfelder, Stefan Tannahill, David
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Methods to measure chromatin contacts at genomic regions bound by histone modifications or proteins are important tools to investigate chromatin organization. However, such methods do not capture the possible involvement of other epigenomic features such as G-quadruplex DNA secondary structures (G4s). To bridge this gap, we introduce ViCAR (viewpoi...
Olan, Ioana Ando-Kuri, Masami Parry, Aled J Handa, Tetsuya Schoenfelder, Stefan Fraser, Peter Ohkawa, Yasuyuki Kimura, Hiroshi Narita, Masako Narita, Masashi
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HMGA1 is an abundant non-histone chromatin protein that has been implicated in embryonic development, cancer, and cellular senescence, but its specific role remains elusive. Here, we combine functional genomics approaches with graph theory to investigate how HMGA1 genomic deposition controls high-order chromatin networks in an oncogene-induced sene...
Dong, Peng Zhang, Shu Gandin, Valentina Xie, Liangqi Wang, Lihua Lemire, Andrew L Li, Wenhong Otsuna, Hideo Kawase, Takashi Lander, Arthur D
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The contrast between the disruption of genome topology after cohesin loss and the lack of downstream gene expression changes instigates intense debates regarding the structure-function relationship between genome and gene regulation. Here, by analyzing transcriptome and chromatin accessibility at the single-cell level, we discover that, instead of ...
Zhao, Shuang Bootsma, Matthew Zhou, Stanley Shrestha, Raunak Moreno-Rodriguez, Thaidy Lundberg, Arian Pan, Chu Arlidge, Christopher Hawley, James Foye, Adam
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The impact of variations in the three-dimensional structure of the genome has been recognized, but solid cancer tissue studies are limited. Here, we performed integrated deep Hi-C sequencing with matched whole-genome sequencing, whole-genome bisulfite sequencing, 5-hydroxymethylcytosine (5hmC) sequencing and RNA sequencing across a cohort of 80 bio...
Kathail, Pooja Shuai, Richard Chung, Ryan Ye, Chun Loeb, Gabriel Ioannidis, Nilah
BACKGROUND: A number of deep learning models have been developed to predict epigenetic features such as chromatin accessibility from DNA sequence. Model evaluations commonly report performance genome-wide; however, cis regulatory elements (CREs), which play critical roles in gene regulation, make up only a small fraction of the genome. Furthermore,...