Table 1. PCR and sequencing primers, in the 5′ to 3′ direction, for the seven loci used in this study.

Gene	Forward	Reverse
Signal peptidase	TTGCCATTTTATGCTGAGCTGAAT	TTTTGGAGCTTCAAGGCTTTATTT
	CCGCTTGTATAGTAGCTGCCATTG	CAACACACAATTAGAACCGTTTTCG
Unknown P1439	GCCTCAAAGAGTGAAAGAGGGTTT	ATCCAGAGGTAGCAAACGGCTTAT
	TCACAGTCCTTTAGCCTGATACTACC
Clathrin light chain	GCCGTGAGGGTCTTTGGTTAAG	CGGTATATAGTATGGGCCTTGGTTC
	TCCTCCATGATAAATGACATGCAA	CAGGAATAGTGCTATCGCGTTCAT
PTTGIIP	TACTTGATCACAGTTCACGCCAAA	CCTATACAGCGCTGATTGCTGATG
Phospholipase A21-precursor	CAGCACGTACTGTGTATCGAAAGAA	AAAAGCAATTTGGAACAAAGTATGAA
	TCATCTGTCGCAGGTACGTATGAA	ACTTGTATCTGGCGAAGCATTCAG
	TTTTGTGCGCGCTAAAACTATCTT
	CTGGTAGCTGTGACCGTGCTAACT
Unknown P1500	ATCCCGCGTTCTCCTACTATTTTT	AATTTTATGATCGCTTCCTGCAAT
	TCATTCGTCGTGTGGCTGTTACTA	GCACAAGTATTAACCACACCGTCA
	GCGCCTTGGTTTCTACTGTTTTGT
Glutathione S-transferase	GGTGTTGCCTTGTGTTCACTTTT	GGGATGCAAAACTAATAATTACCAAA
	TGGTCAAATTCGTCAACTTTACGTTC	TTTCTTAGATTTGGCTGGAAAGAC

The first primer pair for each gene was designed to the 5′ and 3′ UTR; subsequent primers listed below these spanning primers are internal primers. All PCRs were carried out by using the 5′ and 3′ UTR primers and sequencing was performed using all primers listed.