
Transdominant genetics using expression libraries can identify proteins and peptides that affect cell division. In conjunction with these libraries, oligo-nucleotide-conjugated beads and flow cytometry were used to test a strategy that potentially expands the range of such genetic studies. The experimental approach involved creation of tagged expression libraries, introduction of these libraries into cells, growth of the cultured cells for several generations and recovery on oligonucleotide-conjugated beads of sequences that encode growth-modulatory proteins or peptides. Experiments in Saccharomyces cerevisiae demonstrating the feasibility of the strategy are presented.
Base Sequence, Reverse Transcriptase Polymerase Chain Reaction, Oligonucleotides, Combinatorial Chemistry Techniques, Nucleic Acid Hybridization, Saccharomyces cerevisiae, Sensitivity and Specificity, Genes, Dominant
Base Sequence, Reverse Transcriptase Polymerase Chain Reaction, Oligonucleotides, Combinatorial Chemistry Techniques, Nucleic Acid Hybridization, Saccharomyces cerevisiae, Sensitivity and Specificity, Genes, Dominant
| selected citations These citations are derived from selected sources. This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | 13 | |
| popularity This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network. | Average | |
| influence This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | Top 10% | |
| impulse This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network. | Top 10% |
