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. 2018 Oct 4;8(12):3803–3812. doi: 10.1534/g3.118.200527

Table 1. The amino acid (aa) and nucleotide states at the sites of the functionally relevant lysines before the Csd/Fem duplication and divergence event (Csd/Fem MRCA) and before the Csd allele divergence (Csd MRCA).

aa/codon of Csd B2–25 aa/codon of Csd/Fem MRCA (P > 0.9) aa/codon of Csd MRCA (P > 0.9) aa/codon polymorphisms (frequency %)3)
NLS C1 K14 R K K (100%)
AAA AGA AAA AAA
K16 R K K (100%)
AAA AGA AAA AAA
K24 E E E (57%) K (43%)
AAA GAA GAA GAA AAA
C2 K243 Q K K (100%)
AAA CAA AAA AAA
K248 E K E (7%) K (93%)
AAA GAA AAA GAA AAA
C3 K259 R K E (14%) K (79%) N (7%) GAG AAG AAC
AAG AGG AAG2)
K280 E 1) K K (21%) K (79%)
AAG GAA AAA AAG AAA
1)

Ambiguous codon (P < 0.9) due to indels that occurred with outgroup sequence comparison.

2)

The predicted codon was R (AGG), P < 0.6 using ANC-GENE (Zhang and Nei 1997), and K (AAG), P > 0.9 using MEGA (Tamura et al. 2011). From the more parsimonious number of mutations required to produce the other polymorphism (GAG and AAC), we suggest that the aa/codon of the csd MRCA is K/AAG.

3)

Estimated from a random sample of 14 csd alleles.