“…Interestingly, TOP1α not only affects flowering time [16] but also influences seed size (Fig 1A and 1B and S1A Fig). To identify interacting partners of TOP1α, we performed co-immunoprecipitation (CoIP) coupled with liquid chromatography coupled with tandem mass spectrometry (LC-MS/MS) using nuclear extracts of young siliques from the established top1α-10 gTOP1α-4HA line [16]. A peptide corresponding to UPF1 was identified, and the Abbreviations: 3C, chromatin conformation capture; BiFC, bimolecular fluorescence complementation; ChIP, chromatin immunoprecipitation; CoIP, coimmunoprecipitation; CPT, camptothecin; DAP, days after pollination; DRIP, DNA:RNA hybrid immunoprecipitation; FAIRE, formaldehydeassisted isolation of regulatory elements; GUS, βglucuronidase; iku1, haiku1; LC-MS/MS, liquid chromatography coupled with tandem mass spectrometry; mCIP, methyl-cytosine immunoprecipitation; MEG, maternally expressed gene; mini3, miniseed3; NLS, nuclear localization signal; NMD, non-sense mRNA decay; PEG, paternally expressed gene; qPCR, quantitative PCR; SHB1, SHORT HYPOCOTYL UNDER BLUE1; SSP, SHORT SUSPENSOR; TOP1α, TOPOISOMERASE Iα; TTG2, TRANSPARENT TESTA GLABRA2; UPF1, UP-FRAMESHIFT SUPPRESSOR 1; Wa-1, Warschau.…”