Skip to main content
. 1999 Jul 6;96(14):7815–7820. doi: 10.1073/pnas.96.14.7815

Table 1.

Summary of the two-hybrid screens

Bait Transformants tested (×10−6) 3ATR β-Gal+ clones Clone sequenced Transcription complex subunit*
C160 3.0 0 0 None
C128 6.5 0 0 None
C82 24.0 72 39 C34 (1, 1)
C53 13.6 55 38 TFC4 (1, 1); C37 (15, 4)
AC40 50.4 235 109 AC19 (19, 4); A135 (4, 2)
ABC27 7.2 207 118 A190 (12, 10); B220 (2, 1); C160 (7, 6)
C25 15.0 111 71 None
ABC23 5.5 0 0 None
AC19 38.3 450 153 AC40 (6, 5); A135 (3, 2); B44 (2, 2)
ABC14.5 12.0 31 29 B220 (1, 1); C160 (6, 4)
C11 10.6 101 83 C128 (2, 2)
ABC10α 7.3 196 122 A135 (1, 1)
ABC10β 113.2 276 209 B220 (1, 1); B150 (2, 1)
TFIIIB70 9.2 96 82 TFC4 (2, 2)
A12.2 11.0 105 82 A135 (1, 1)
B12.5 19.3 302 185 B44 (27, 18)
*

The numbers between the parentheses represent the total number of selected clones and the number of independent clones, respectively. 

Only 320 of the 968 3ATR clones selected in the AC40 screen and 632 of the 2,136 3ATR clones selected in the AC29 screen were tested for β-galactosidase production.