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Table 1 Differential expression of proteins from fins by 2D-DIGE (Exp1, Exp2 and Exp3) and of their corresponding transcripts by hybridization to oligo microarrays

From: Zebrafish fin immune responses during high mortality infections with viral haemorrhagic septicemia rhabdovirus. A proteomic and transcriptomic approach

Spot n°

Protein Name

Accession Number

~MW ×10-3

~pI

fold

Exp1

fold

Exp2

fold

Exp3

microarray

SIGNALING

47

hmgb1

42476233

16

7.0

2.4

*3.7

---

1.01

26

gnb1 (G prot), βpolypep1

47087315

35

5.6

2.6

3.0

---

1.03

APOPTOSIS

27

Annexin A1a

31419751

40

6.0

2.3

9.1

---

1.01

39

Annexin 1a

27762256

44

6.2

2.5

---

---

N.F.

0

Annexin A5b

41107552

36

5.2

---

---

-2.0

-1.08

0

Annexin 5b

160773369

36

5.3

---

---

-1.9

N.F.

DETOXIFICATION

34

Glutathion S-Transferase

18858197

16

8.2

11.0

*2.7

---

1.30

32

Glutathion S-Transferase

47086689

20

6.4

4.0

*2.1

---

1.30

HAEMATOPOIESIS

10

Transferrin

51859259

70

6.9

16.1

*4.6

---

2.40

11

Hemopexin

33991748

65

6.3

2.5

*3.2

---

5.42

12

Hemopexin

33991748

65

6.5

3.5

---

---

5.42

GLYCOLYSIS & ATP

24

Aldolase fructose-bisphosphate

37595414

44

8.3

5.7

8.2

*1.4

1.15

45

Triosephosphate isomerase 1b

47271422

18

7.1

2.1

*1.5

1.5

1.00

29

GAPDH

56718619

42

7.2

5.3

10.2

*1.8

1.12

31

GADPH

53733367

40

8.2

4.2

8.7

---

1.12

4

GAPDH

53733367

85

5.6

-7.4

---

-*1.7

1.12

16

Alpha enolase 1

37681795

57

6.7

6.0

17.6

1.8

1.18

28

Ldhb Lactate dehydrogenase

28277619

35

6.8

3.3

---

*2.2

1.04

33

Carbonic anhydrase

18858379

22

7.8

10.4

---

---

-1.04

43

Malate dehydrogenase

47085883

40

7.8

2.1

*1.7

---

1.05

3

ATP binding

51571925

85

5.5

-19.1

---

---

-2.22

0

ATP synthase

41152334

24

7.0

---

---

1.5

1.05

46

Creatine kinase

55716037

15

6.5

-3.4

---

-*1.7

3.16

20

Creatine kinase

55716037

48

6.4

-3.9

---

-*2.0

3.16

5

Creatine kinase

55716037

90

5.9

-4.0

---

-*2.0

3.16

CYTOSKELETON & RELATED PROTEINS

42

Keratin 18

41351240

57

5.3

3.2

11.2

---

1.08

38

Keratin type I

50370316

57

5.6

2.4

---

---

1.09

13

Type II cytokeratin

18858425

59

5.1

3.2

1.0

---

1.23

50

Tubulin, gamma assoc protein 2

41056243

85

6.0

2.4

---

---

-1.01

30

Skeletal alpha-actin (S. aurata)

6653228

38

7.9

-2.7

-2.8

---

-1.53

21

Alpha-tropomyosin

18859505

44

6.6

---

3.4

7.2

1.56

0

Alpha-tropomyosin

55962544

36

5.0

---

---

11.7

1.56

15

Transgelin

37681953

49

5.2

-7.4

---

---

1.49

22

Kinesin-like protein

50055013

50

6.7

-2.7

---

---

-2.5

41

Myosin VIa

10116291

114

5.9

2.0

*5.1

7.7

1.05

0

Myosin, light chain 2

18859049

22

5.0

---

---

7.3

1.30

19

CapG

29612467

48

5.3

2.8

*7.6

---

-1.08

0

Actin capping protein

41053959

34

5.7

---

---

-1.6

1.09

6

Scinderin

42542770

80

6.4

4.1

---

---

-1.14

7

Scinderin

42542770

80

6.5

3.8

---

---

-1.14

17

Cyclase-associated protein-1

37725381

58

8.3

5.0

---

---

1.66

35

Dynamin 1-like

41055508

5

5.3

3.0

---

---

1.01

48

Semaphorin 3Gb

57790316

7

6.4

3.0

---

---

1.09

14

CkII protein

39645432

65

5.3

2.9

---

---

1.13

0

fgf20 fin regeneration

51571925

26

6.2

---

---

1.8

1.26

0

fgf20 fin regeneration

51571925

26

6.9

---

---

2.2

1.26

0

fgf20 fin regeneration

51571925

26

7.0

---

---

2.3

1.26

0

fgf20 fin regeneration

51571925

26

7.2

---

---

1.8

1.26

  1. Exp1, experiment 1. Exp2, experiment 2. Exp3, experiment 3. Spot n°, number of spot selected in the 2 D gel of Exp1 (Figure 2) for mass spectrophotometry (MS) identification. 0, numbers of spots selected in 2 D gels of exp 2 or 3 (not shown). Gel spots were digested with trypsin and their peptides identified by MS. The corresponding detected proteins with a 100% of probability score of identification are shown grouped by their function. *, spots hypothetically identified by their apparent molecular weight (MW) and isoelectric point (IP) in their respective 2 D gels. ---, spots too faint to be quantified. ~MW and ~PI, apparent molecular weight (MW) and isoelectric points (IP) in the 2 D gel. Accession number of the identified protein sequences in the protein bank. Fold, calculated by the DeCyder-differential in-gel analysis software by the formula, volume of the spot in the VHSV-infected fin/volume of the spot in the non-infected fin. The spots on Figure 2 which have no corresponding description on Table 2 could not be identified by MS. Microarray differential expression data was obtained as explained in the legend of Table 3. Because most of the protein genes appeared several times in the microarray, their corresponding folds were calculated as the means for each of their data (n = 3-10). NF, not found annotated in the microarray.