Supplemental Data TABLE 1 Viability Counts A. Progeny from crossing cry0/TM6B to Df(3R)Dl-Bx12/MKRS Df/TM6B cry0/MKRS cry0/Df TM6B/MKRS ________________________________________________________________________ Count 70 1210 898 467 Ratio - 2.6 1.9 1.0 B. Control for A: cry+/TM6B x Df/MKRS Df/TM6B cry+/MKRS cry+/Df TM6B/MKRS ________________________________________________________________ Count 0 203 98 60 Ratio - 3.4 1.6 1.0 C. Progeny from Mendelian test: cry0/cry+ x cry0/cry+ cry0/cry+ cry0/cry0 cry+/cry+ ________________________________________________________________ Count 167 85 72 Ratio 2.3 1.2 1.0 For each of the three types of crosses, the lefthand parental genotype was carried in females, the righthand one in males. With regard to A and B, the deletion (Df) of the cry locus and the 3rd-chromosomal balancers (TM6B and MKRS) are specified in MATERIALS AND METHODS; the cry-null mutations were from the cry01 and cry02 strains (used in separate crosses that led to the data in A), and the cry+ allele (B) was from the isoW strain (see MATERIALS AND METHODS). The ratios involving progeny from A and B crosses were computed with respect to numbers of balancer-over-balancer progeny set equal to 1.0. These calculations ignored numbers of the Df/TM6 offspring (thus the “-” entries), because flies of that doubly-defective genotype exhibited erratic and very low adult-emergence probabilities overall. Putative reason: combined effects of heterozygosity for this Df (a deletion that removes genes in addition to the cry one) and the dominant marker contained in the TM6 balancer. Inferentially, other fly types carrying this Df are have their viability impinged upon, irrespective of the cry allele carried on the homologous 3rd chromosome; hence, the ratio method for computing relative viabilities as affected by uncoverage of cry0 by this deletion, vis-à-vis heterozygosity for the Df and cry+. That number for the cry0/Df offspring is clearly robust in comparison to the cry+/Df control value. For cross C, the genetic background of the parents was w1118; the three progeny types were scored by virtue of the w+-inserted cry0’s leading to darker eye color in homozygotes compared with cry0/+ heterozygotes; note that a classical F2 Mendelian ratio was realized; again, this indicates no deleterious effect of the cry-null mutation on viability.