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. 2016 Aug 2;6(10):3139–3148. doi: 10.1534/g3.116.032300

Table 1. Testing viability of chromosomal pairing factor knockdown in vivo.

Adult Viability with shRNA Expression
Gene BDSC shRNA Stock Number Cha-GAL4 > shRNA α-tubulin-GAL4 > shRNA
CG2469 33,736 N/a
chb 34,669 N/a
Dhc64C 36,698 N/a
Klp61f 33,685 N/a
Nlp 33,688 N/a
shtd 38,531 N/a
SkpA 32,991 N/a
slmb 33,986 N/a
Tlk 33,983 N/a
Arp1 32,032 +
aurB 28,691 +
cal1 41,716 +
CG7236 27,505 +
CKIα 25,786 +
Cul1 29,520 +
Det 51,837 +
E(bx) 33,658 +
fzy 40,933 +
Hsc70Cb 33,742 + +
ida 34,552 +
Lis-1 35,043 +
Nc73EF 33,686 +
pbl 28,343 +
polo 33,042 +
su(Hw) 34,006 + +
w 33,623 + +

shRNAs from the TRiP library against the listed genes, which have been identified in previous studies as playing a role in somatic homolog pairing, were obtained from the BDSC. shRNA expression was driven in cholinergic neurons with the Cha-GAL4 driver, or ubiquitously with the α-tubulin-GAL4 driver. shRNA against the w gene was included as a positive control. shRNA, short hairpin RNA; BDSC, Bloomington Drosophila Stock Center; −, no viable adult flies recovered; N/a, cross not performed; +, viable adult flies recovered; TRiP, Transgenic RNA Interference Project.