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. 1998 Mar 31;95(7):3752–3757. doi: 10.1073/pnas.95.7.3752

Table 1.

Yeast ORFs identified by array analysis of two-hybrid screens

Clone type YMR117c YMR138w (CIN4)
Genes YBR020w YDL117w
YCL032W (STE50) YDR087c
YCR073c (SSK22) YGL172w (NUP49)
YDR104c YHR141c (MAK18)
YER018c YLR109w
YER032w (FIR1) YNR050c (LYS9)
YFR046c YPL241c (CIN2)
YGL197w
YIL144w
YLR319c (BUD6)
YLR419w
YML049c
YMR224c (MRE11)
YOL18c
YOL34w
YOR206w
YPR010c (RPA135)
YPR145w (ASN1)
DNA not encoding protein 18S and 25S rRNA
Reverse orientation YNL291c YBR189w
YDR381w
YNL301c (RP28B)
YNR035c
YOL056w (GPM3)

ORF loci and names are listed for genes detected by array hybridization of PCR products derived from end products of a two-hybrid screen. Because inserts in the noncoding orientation comprise a significant proportion of false positives in the two-hybrid screen, RNA was transcribed from the upstream T7 promoter and used to generate exclusively antisense cDNA strands with reverse transcriptase. cDNA products were then biotinylated, fragmented, and hybridized as described. Genes detected by a double-stranded DNA hybridization but absent in cDNA hybridization are considered to be in reverse orientation. Control experiments were performed to confirm that this method is orientation-specific (data not shown).