scholarly journals Long-Term Safety and Tolerability of BMP7 and HGF Gene Overexpression in Rabbit Cornea

2021 ◽  
Vol 10 (10) ◽  
pp. 6
Author(s):  
Suneel Gupta ◽  
Nishant R. Sinha ◽  
Lynn M. Martin ◽  
Landon M. Keele ◽  
Prashant R. Sinha ◽  
...  
1988 ◽  
Vol 89 (1) ◽  
pp. 91-97 ◽  
Author(s):  
J. Čeiková ◽  
Z. Lojda ◽  
B. Brůnová ◽  
J. Vacík ◽  
J. Michálek

Author(s):  
Kobayashi Hisatoshi ◽  
Hattori Shinya ◽  
Honda Takako ◽  
Kameda Tsunenori ◽  
Tamada Yasushi
Keyword(s):  

2021 ◽  
Author(s):  
DeElegant Robinson ◽  
Michael Place ◽  
James Hose ◽  
Adam Jochem ◽  
Audrey P Gasch

Copy number variation (CNV) through gene or chromosome amplification provides a route for rapid phenotypic variation and supports long-term evolution of gene functions. Although the evolutionary importance of CNV is known, little is understood about how genetic background influences CNV tolerance. Here, we measured fitness costs of over 4,000 over-expressed genes in 15 Saccharomyces cerevisiae strains representing different lineages, to explore natural variation in tolerating gene overexpression (OE). Strain-specific effects dominated the fitness costs of gene OE. We report global differences in the consequences of gene OE, independent of the amplified gene, as well as gene-specific effects that were dependent on the genetic background. Natural variation in the response to gene OE could be explained by several models, including strain-specific physiological differences, resource limitations, and regulatory sensitivities. This work provides new insight on how genetic background influences tolerance to gene amplification and the evolutionary trajectories accessible to different backgrounds.


Cornea ◽  
2004 ◽  
Vol 23 (Supplement 1) ◽  
pp. S87-S90 ◽  
Author(s):  
Takahiro Kiuchi ◽  
Hideo Tatsuzaki ◽  
Taketoshi Wakabayashi ◽  
Fumiki Okamoto ◽  
Yuichi Kaji ◽  
...  

eLife ◽  
2021 ◽  
Vol 10 ◽  
Author(s):  
DeElegant Robinson ◽  
Mike Place ◽  
James Hose ◽  
Adam Jochem ◽  
Audrey P Gasch

Copy number variation (CNV) through gene or chromosome amplification provides a route for rapid phenotypic variation and supports long-term evolution of gene functions. Although the evolutionary importance of CNV is known, little is understood about how genetic background influences CNV tolerance. Here, we measured fitness costs of over 4,000 over-expressed genes in 15 Saccharomyces cerevisiae strains representing different lineages, to explore natural variation in tolerating gene overexpression (OE). Strain-specific effects dominated the fitness costs of gene OE. We report global differences in the consequences of gene OE, independent of the amplified gene, as well as gene-specific effects that were dependent on the genetic background. Natural variation in the response to gene OE could be explained by several models, including strain-specific physiological differences, resource limitations, and regulatory sensitivities. This work provides new insight on how genetic background influences tolerance to gene amplification and the evolutionary trajectories accessible to different backgrounds.


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