. 2016 Sep 20;113(39):11028–11033. doi: 10.1073/pnas.1605588113

Table S1.

Primers used for cloning and RT-PCR analysis

DNA region	Primer	Sequence 5′–3′
Cloning
Genomic PEPR1	Forward	GGGGACAAGTTTGTACAAAAAAGCAGGCTCAATGAAGAATCTTGGGGGGTTGTTC
Genomic PEPR1	Reverse	GGGGACCACTTTGTACAAGAAAGCTGGGTACCGAACTGAATCAGAGGAGCA
Genomic PEPR2	Forward	GGGGACAAGTTTGTACAAAAAAGCAGGCTCAATGAGGAATCTTGGGTTACTCG
Genomic PEPR2	Reverse	GGGGACCACTTTGTACAAGAAAGCTGGGTAGTGAACTGAACCCGAAGTGCTTCT
Promoter PEPR1	Forward	GGGGACAACTTTGTATAGAAAAGTTGCTTCACTGATCTGTTTGTTGCAAAC
Promoter PEPR1	Reverse	GGGGACTGCTTTTTTGTACAAACTTGCCTGAGTTTAAAGATCGAGAAACATG
Promoter PEPR2	Forward	GGGGACAACTTTGTATAGAAAAGTTGCTATTAGGGTGGTCTATCGGTCAG
Promoter PEPR2	Reverse	GGGGACTGCTTTTTTGTACAAACTTGCATTAGAGCTCAAGAGACTGAAATATG
CDS Auxilin2	Forward	CACCATGGATGATTTCACAGGATTGTT
	Reverse	TCAAAAGAGTTCCTCTGAGTTGAAT
RT-PCR
GAPDH	Forward	TTGGTGACAACAGGTCAAGCA
GAPDH	Reverse	AAACTTGTCGCTCAATGCAA
PEPR1	Forward	GTTTTGGCTGAGGAAAGACG
PEPR1	Reverse	ACATTGTACCGTGCAGACCA