Supplementary material for Brown et al., Proc. Natl. Acad. Sci. USA, 10.1073/pnas.120184097
Table 1.
ApoB48R intronic sequences and location identified by PCR cloning using THP-1 monocyte-macrophage genomic DNA as templateIntron 1 (360 bp) between bp 67 and 68 of the cDNA, Fig. 8 |
GT GAGAAGGGCAGACAGCTGCCAGATACTTGCACCCCATTCCCTGGGGCCTCACTTCCGGGCACCTCCCCTGGGGCCTCACCTTTCCCCTCCTCCTTCTGATCTCCTCTAACTGGA GATTGCTTTCTCAGGTTCAGGCAGACTCCTGGCCTAATATTTTCTGAATTTCAGTCCC CACCTCCAACCATGCGTCCTCGTACCCCTAATCGATGCCCCTTCTGGCTCCTTCTGCA AATCCTCTTCTTCTCCTTTCAGATCCCAGTACCCTCTTCCTTAACCTGGGCTCCTCCA GCCAGGGCCCCCAGGGAAAGGGCTGGGACTCTCCTCAATGACTCTCCCCTCTCTCTCT CTTTTTTCCTAG |
Intron 2 (84) between bp 3,228 and 3,229 of the cDNA, Fig. 8 |
GT GAGGGCTCTTGGTGGGGTCTCGGGGGGAACGAGTGGAATCCCGAAGCCGGCCCCATGGTCCTCTGTGCCCCCTTTCCTGCAG |
Intron 3 (86) between bp 3,207 and 3,208 of the cDNA, Fig. 8 |
GT GAGGGCTCTTGGTGGGGTCTCGGGGGGAACGAGTGGAATCCCGAAGCCGGCCCCATGGTCCTCTGTGCCCCCTTTCCTGCAG |
Underlining indicates intron-exon boundary motif GT. . . AG.