Table 1. Summary of primers used in this study.

Primers	Primer sequence (5′-3′)
Overexpression assay
111L-GFP-F	CGGAATTCATGGAACTGTGTCAGCCC
111L-GFP-R	CGGGATCCGAGATCGCACACGTGTA
RFP-111L-F	GGGGTACCATGGAACTGTGTCAGCC
RFP-111L-R	CGGGATCCGAGATCGCACACGTG
111-RNA-F	ATGGACTACAAAGACGATGACGACAAGATGGAACTGTGTCAGCCCAACAAC
111-RNA-R	CTAGAGATCGCACACGTGTACCTTGAT
GST Pulldown assay
GST-111L-F	CGGGATCCATGGAACTGTGTCAGCCC
GST-111L-R	CGGAATTCGAGATCGCACACGTGTA
MYC-TRADD-F	GGGGTACCAATGGACAGTATAGACACAAAGAGG
MYC-TRADD-R	CGGGATCCTTAATCTCGTGGCTGGAT
RT-qPCR assay
β-actin-QF	ATGCCCCTCGTGCTGTTTTC
β-actin-QR	GCCTCATCTCCCACATAG GA
caspase 8-QF	AGACCAGGAACAAGGAGGCAGACT
caspase 8-QR	CTGTAGTAATTGTGCCAGCCGAAGAG
ISH riboprobe synthesis
caspase 8-PF	CGGAATTCCTGACAAGCGGTGATGTGGACC
caspase 8-PR	GGGGTACCCATATCAGTGCCTGTTCGTTTGAGC
caspase 3-PF	ATGCAGGTTGATGCCAAGCCT
caspase 3-PR	TGAACAGACTAGTTAAAGACTTGAGATCCAC
Morpholino assay
MO-caspase 8-F	CTGACAAGCGGTGATGTGGA
MO-caspase 8-R	GCCCAAGCCTCTGTTGTTTT
MO-β-actin-F	GACGACCCAGACATCAGGGAGTG
MO-β-actin-R	TGGAGTTGAAGGTGGTCTCGTGGA

The underlined letters is the restriction endonuclease cutting site.