A genome wide dosage suppressor network reveals genomic robustness

作者：Patra Biranchi; Kon Yoshiko; Yadav Gitanjali; Sevold Anthony W; Frumkin Jesse P; Vallabhajosyula Ravishankar R; Hintze Arend; Ostman Bjorn; Schossau Jory; Bhan Ashish; Marzolf Bruz; Tamashiro Jenna K; Kaur Amardeep; Baliga Nitin S; Grayhack Elizabeth J; Adami Christoph; Galas David J; Raval Alpan; Phizicky Eric M; Ray Animesh^*

来源：Nucleic Acids Research, 2017, 45(1): 255-270.

DOI：10.1093/nar/gkw1148

Genomic robustness is the extent to which an organism has evolved to withstand the effects of deleterious mutations. We explored the extent of genomic robustness in budding yeast by genome wide dosage suppressor analysis of 53 conditional lethal mutations in cell division cycle and RNA synthesis related genes, revealing 660 suppressor interactions of which 642 are novel. This collection has several distinctive features, including high cooccurrence of mutant-suppressor pairs within protein modules, highly correlated functions between the pairs and higher diversity of functions among the co-suppressors than previously observed. Dosage suppression of essential genes encoding RNA polymerase subunits and chromosome cohesion complex suggests a surprising degree of functional plasticity of macromolecular complexes, and the existence of numerous degenerate pathways for circumventing the effects of potentially lethal mutations. These results imply that organisms and cancer are likely able to exploit the genomic robustness properties, due the persistence of cryptic gene and pathway functions, to generate variation and adapt to selective pressures.

• 出版日期2017-1