TY - JOUR
T1 - High-throughput replica-pinning approach to screen for yeast genes controlling low-frequency events
AU - Novarina, Daniele
AU - Bringas, Fernando R. Rosas
AU - Rosas Bringas, Omar
AU - Chang, Michael
N1 - Funding Information:
F.R.R.B. was supported by a CONACYT scholarship.
Publisher Copyright:
© 2021 The Author(s)
PY - 2022/3/18
Y1 - 2022/3/18
N2 - Saccharomyces cerevisiae is a leading model system for genome-wide screens, but low-frequency events (e.g., point mutations, recombination events) are difficult to detect with existing approaches. Here, we describe a high-throughput screening technique to detect low-frequency events using high-throughput replica pinning of high-density arrays of yeast colonies. This approach can be used to screen genes that control any process involving low-frequency events for which genetically selectable reporters are available, e.g., spontaneous mutations, recombination, and transcription errors. For complete details on the use and execution of this protocol, please refer to (Novarina et al., 2020a, 2020b).
AB - Saccharomyces cerevisiae is a leading model system for genome-wide screens, but low-frequency events (e.g., point mutations, recombination events) are difficult to detect with existing approaches. Here, we describe a high-throughput screening technique to detect low-frequency events using high-throughput replica pinning of high-density arrays of yeast colonies. This approach can be used to screen genes that control any process involving low-frequency events for which genetically selectable reporters are available, e.g., spontaneous mutations, recombination, and transcription errors. For complete details on the use and execution of this protocol, please refer to (Novarina et al., 2020a, 2020b).
U2 - 10.1016/j.xpro.2021.101082
DO - 10.1016/j.xpro.2021.101082
M3 - Article
SN - 2666-1667
VL - 3
JO - STAR protocols
JF - STAR protocols
IS - 1
M1 - 101082
ER -