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. 2019 Jan 23;116(6):2193–2199. doi: 10.1073/pnas.1819020116

Table 4.

Alternative splicing events predicted from prp-8 G654E mRNA-Seq analysis

Genotype Up 5′SS use str. 1,2, %
Gene & Sequence: T12C9.7; TTTATTTCTGGTTgtgagaatttgttttatagttt
 snrp-27(+); prp-8(+) 18.65, 18.74
 snrp-27(M141T); prp-8(+) 97.55, 95.55
 snrp-27(+); prp-8(G654E) 35.61, 35.83
 snrp-27(+); prp-8(T524S) 1.41, 1.12
Gene & Sequence: stip-1; AGGATCAGGCGACATAT GGTGGGgtgagatcattgaaaa
 snrp-27(+); prp-8(+) 75.96, 75.74
 snrp-27(M141T); prp-8(+) 94.46, 95.54
 snrp-27(+); prp-8(G654E) 92.63, 91.88
 snrp-27(+); prp-8(T524S) 86.61, 87.07
Gene & Sequence: spat-2; AACAGCGTTGTGAGG ATGGCCTTGCAAGAAGGGgtgcgggctta
 snrp-27(+); prp-8(+) 71.76, 72.07
 snrp-27(M141T); prp-8(+) 45.43, 42.86
 snrp-27(+); prp-8(G654E) 59.26, 61.84
 snrp-27(+); prp-8(T524S) 50.34, 51.64

Sequences of the alternative spliced regions. 5′ SSs promoted in prp-8 mutant indicated by a filled triangle, partner 5′ SS indicated by an open triangle. Uppercase are sequences that can be exons; lowercase are always intronic. Below the sequence is quantitation of alternative 5′ splice-site usage by 32P-RT-PCR analysis. Genotypes are indicated. T12C9.7 was identified in the prp-8 G654E library, stip-1 in both prp-8 libraries, and spat-2 in the prp8 T524S library.