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Table 7 Rate of evolution of ESE and (a) non-ESE sequence and (b) pseudoESE sequence at four-fold degenerate sites

From: The evolution, impact and properties of exonic splice enhancers

Dataset

Median ESE

Median non-ESE

% Difference

Ptwo-sided

A

ESR

0.3

0.39

-23.1

1.10E-13

INT2.400

0.32

0.36

-11.1

1.10E-13

INT3

0.3

0.36

-16.7

1.10E-13

INT3.400

0.3

0.35

-14.2

1.10E-13

INT3_ESR

0.3

0.35

-14.2

1.10E-13

INT3_ESR_400

0.29

0.35

-17.1

3.40E-13

Ke-ESE

0.35

0.34

2.9

8.20E-08

Ke-ESE400

0.38

0.34

11.8

1.10E-13

PESE

0.31

0.37

-16

1.10E-13

RESCUE

0.32

0.35

-8.5

5.70E-13

B

    

ESR

0.3

0.35

-14.3

4.50E-13

INT2.400

0.32

0.35

-8.5

4.50E-13

INT3

0.3

0.35

-14.3

4.50E-13

INT3.400

0.3

0.34

-11.8

4.50E-13

INT3_ESR

0.3

0.34

-11.8

4.50E-13

INT3_ESR_400

0.29

0.34

-14.7

2.30E-12

Ke-ESE

0.35

0.35

0

4.10E-06

Ke-ESE400

0.38

0.36

5.6

4.50E-13

PESE

0.31

0.35

-11.4

4.50E-13

RESCUE

0.32

0.35

-8.5

4.50E-13

  1. We consider the proportion of four fold degenerate sites that are changed or unchanged when comparing mouse-human alignments. We split sites by whether in human the sequence matches an ESE or not (Table A) or ESE versus pseudoESE (Table B). We then perform a Wilcoxon paired test considering the rate of evolution of ESE and non-ESE or pseudoESE at each position away from an exon boundary. We also present the % difference between the medians, this being (median for ESE - median for non-ESE)/median for non-ESE. All tests are significant after Bonferonni correction (for consistency the P values are shown in bold).