scholarly journals Single-Cell Tracing Dissects Regulation of Maintenance and Inheritance of Transcriptional Reinduction Memory

2020 ◽  
Vol 78 (5) ◽  
pp. 915-925.e7 ◽  
Author(s):  
Poonam Bheda ◽  
Diana Aguilar-Gómez ◽  
Nils B. Becker ◽  
Johannes Becker ◽  
Emmanouil Stavrou ◽  
...  
Keyword(s):  
2019 ◽  
Vol 16 (11) ◽  
pp. 1123-1130 ◽  
Author(s):  
Christoph Thiele ◽  
Klaus Wunderling ◽  
Philipp Leyendecker

2009 ◽  
Vol 113 (18) ◽  
pp. 6511-6519 ◽  
Author(s):  
Valentin Lulevich ◽  
Yi-Ping Shih ◽  
Su Hao Lo ◽  
Gang-yu Liu

2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Raquel Rouco ◽  
Olimpia Bompadre ◽  
Antonella Rauseo ◽  
Olivier Fazio ◽  
Rodrigue Peraldi ◽  
...  

AbstractDevelopmental genes are frequently controlled by multiple enhancers sharing similar specificities. As a result, deletions of such regulatory elements have often failed to reveal their full function. Here, we use the Pitx1 testbed locus to characterize in detail the regulatory and cellular identity alterations following the deletion of one of its enhancers (Pen). By combining single cell transcriptomics and an in-embryo cell tracing approach, we observe an increased fraction of Pitx1 non/low-expressing cells and a decreased fraction of Pitx1 high-expressing cells. We find that the over-representation of Pitx1 non/low-expressing cells originates from a failure of the Pitx1 locus to coordinate enhancer activities and 3D chromatin changes. This locus mis-activation induces a localized heterochrony and a concurrent loss of irregular connective tissue, eventually leading to a clubfoot phenotype. This data suggests that, in some cases, redundant enhancers may be used to locally enforce a robust activation of their host regulatory landscapes.


Author(s):  
Cheng-Yu Fan ◽  
Tsai Chia-Jung ◽  
Lin Hsuan-Chao ◽  
Yu Ling-Yea ◽  
Hsiao Yung-Jen ◽  
...  

2007 ◽  
Vol 58 ◽  
pp. S212
Author(s):  
Kouichi Nakamura ◽  
Fumino Fujiyama ◽  
Takahiro Furuta ◽  
Takeshi Kaneko

Author(s):  
Debby A. Jennings ◽  
Michael J. Morykwas ◽  
Louis C. Argenta

Grafts of cultured allogenic or autogenic keratlnocytes have proven to be an effective treatment of chronic wounds and burns. This study utilized a collagen substrate for keratinocyte and fibroblast attachment. The substrate provided mechanical stability and augmented graft manipulation onto the wound bed. Graft integrity was confirmed by light and transmission electron microscopy.Bovine Type I dermal collagen sheets (100 μm thick) were crosslinked with 254 nm UV light (13.5 Joules/cm2) to improve mechanical properties and reduce degradation. A single cell suspension of third passage neonatal foreskin fibroblasts were plated onto the collagen. Five days later, a single cell suspension of first passage neonatal foreskin keratinocytes were plated on the opposite side of the collagen. The grafts were cultured for one month.The grafts were fixed in phosphate buffered 4% formaldehyde/1% glutaraldehyde for 24 hours. Graft pieces were then washed in 0.13 M phosphate buffer, post-fixed in 1% osmium tetroxide, dehydrated, and embedded in Polybed 812.


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