Files in this data supplement:

• Supporting Information: Figures S1-S8, Tables S1 and S2, and Files S1 and S2 (PDF, 7.6 MB)
• Figure S1: OMA-1 reorganizes into large RNPs when sperm-dependent signaling is compromised (PDF, 962 KB)
• Figure S2: Purification strategies used to characterize OMA-1-interacting mRNAs (left) and proteins (right) (PDF, 76 KB)
• Figure S3: Previously identified mRNA targets of OMA-dependent translational repression appear to be abundant in OMA-1 purifications (PDF, 1.1 MB)
• Figure S4: OMA-1-associated 3?UTRs that are weakly repressed or not regulated by OMA-1/2 (PDF, 1.2 MB)
• Figure S5: Different patterns of GFP::H2B expression from the 3'UTR reporter transgenes described in the text (PDF, 1.5 MB)
• Figure S6: GFP::H2B expression from reporter transgenes is not dramatically altered in oocytes with a reduced rate of oocyte maturation (PDF, 1.6
• Figure S7: GFP::H2B expression from reporter transgenes is increased in fog-2(oz40) females after oma-1/2(RNAi) (PDF, 558 KB)
• Figure S8: Overlapping sets of proteins were identified in OMA-1 purifications (PDF, 761 KB)
• Table S1: C. elegans strains used for this study (PDF, 99 KB)
• Table S2: Relative quantification of zif-1 and nos-2 target mRNA levels in OMA-1 purifications (IPs) using RT-PCR and RNA sequencing (PDF, 69 KB)
• File S1: Identification and analysis of OMA-1-associated mRNAs (.xlsx, 2 MB)
• File S2: Identification and analysis of OMA-1-associated proteins (.xlsx, 56 KB)