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Table 1 Quantitative assessment of phenotypic rescue of moe- mutant defects by injection of moe and epb4.1l5 mRNA constructs.

From: Tissue-specific requirements for specific domains in the FERM protein Moe/Epb4.1l5 during early zebrafish development

Injected mRNA Construct

Genetic Background

% Edema

% Brain Ventricle Defects

% RPE Defects

Apical ZO-1/panCrb

Retinal Lamination

-

wt control

0% (0/81)

0% (0/81)

0% (0/81)

Yes

Yes

-

moe+/- incross

25% (22/88)

25% (22/88)

25% (22/88)

No

No

moe

moe+/- incross

24% (8/34)

0% (0/34)

0% (0/34)

Yes

Yes

epb4.1l5 long

moe+/- incross

25% (6/24)

0% (0/24)

0% (0/24)

Yes

Yes

epb4.1l5 short

moe+/- incross

27% (10/37)

27% (10/37)

24% (9/37)

No

No

epb4.1l5 FERM

moe+/- incross

24% (4/17)

24% (4/17)

24% (4/17)

No

No

epb4.1l5 long_ΔPBD

moe+/- incross

26% (30/86)

26% (30/86)

26% (30/86)

No

No

epb4.1l5 short+long_PBD

moe+/- incross

19% (9/48)

23% (11/48)

0% (0/48)

Yes

Yes

epb4.1l5 long+short_PBD

moe+/- incross

61% (20/47)

96% (54/56)

1% (1/88)*

Yes

Yes

epb4.1l5 long

wt

0% (0/16)

0% (0/16)

0% (0/16)

NA

NA

epb4.1l5 long+short_PBD

wt

20% (7/35)

42% (32/63)

3% (1/35)

NA

NA

  1. Wild-type embryos or embryos from heterozygous moe+/- incrosses were injected with the indicated mRNA constructs and scored based on pericardial edema, brain ventricle defects, RPE defects, apical localization of ZO-1 or Crb2a at 30 hpf, and retinal lamination at 5 dpf. Phenotypes that were not analyzed are indicated with an NA. * See Figure 4M, N and text.