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  • Consequences of a telomerase-related fitness defect and chromosome substitution technology in yeast synIX strains.

Consequences of a telomerase-related fitness defect and chromosome substitution technology in yeast synIX strains.

Cell genomics (2023-11-29)
Laura H McCulloch, Vijayan Sambasivam, Amanda L Hughes, Narayana Annaluru, Sivaprakash Ramalingam, Viola Fanfani, Evgenii Lobzaev, Leslie A Mitchell, Jitong Cai, Hua Jiang, John LaCava, Martin S Taylor, William R Bishai, Giovanni Stracquadanio, Lars M Steinmetz, Joel S Bader, Weimin Zhang, Jef D Boeke, Srinivasan Chandrasegaran
摘要

We describe the complete synthesis, assembly, debugging, and characterization of a synthetic 404,963 bp chromosome, synIX (synthetic chromosome IX). Combined chromosome construction methods were used to synthesize and integrate its left arm (synIXL) into a strain containing previously described synIXR. We identified and resolved a bug affecting expression of EST3, a crucial gene for telomerase function, producing a synIX strain with near wild-type fitness. To facilitate future synthetic chromosome consolidation and increase flexibility of chromosome transfer between distinct strains, we combined chromoduction, a method to transfer a whole chromosome between two strains, with conditional centromere destabilization to substitute a chromosome of interest for its native counterpart. Both steps of this chromosome substitution method were efficient. We observed that wild-type II tended to co-transfer with synIX and was co-destabilized with wild-type IX, suggesting a potential gene dosage compensation relationship between these chromosomes.

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Sigma-Aldrich
单克隆抗-FLAG® M2 小鼠抗, 1 mg/mL, clone M2, affinity isolated antibody, buffered aqueous solution (50% glycerol, 10 mM sodium phosphate, and 150 mM NaCl, pH 7.4)
Sigma-Aldrich
羟基脲, 98%, powder
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(S)-(+)-喜树碱, ≥90% (HPLC), powder