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HAL Id: hal-02934553

https://hal.sorbonne-universite.fr/hal-02934553

Submitted on 9 Sep 2020

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Freezing activity brief data from a new FUS mutant

zebrafish line

Maria-Letizia Campanari, Annis-Rayan Bourefis, Valerie Buee-Scherrer, Edor

Kabashi

To cite this version:

Maria-Letizia Campanari, Annis-Rayan Bourefis, Valerie Buee-Scherrer, Edor Kabashi. Freezing

ac-tivity brief data from a new FUS mutant zebrafish line. Data in Brief, Elsevier, 2020, 31, pp.105921.

�10.1016/j.dib.2020.105921�. �hal-02934553�

(2)

Contents lists available at ScienceDirect

Data

in

Brief

journal homepage: www.elsevier.com/locate/dib

Data

Article

Freezing

activity

brief

data

from

a

new

FUS

mutant

zebrafish

line

Maria-Letizia

Campanari

a

,

b

,

1

,

Annis-Rayan

Bourefis

a

,

b

,

1

,

Valerie

Buee-Scherrer

c

,

Edor

Kabashi

a

,

b

,

a Imagine Institute, Institut National de la Santé et de la Recherche Médicale (INSERM) Unité 1163, Paris Descartes

Université, Paris 75015, France

b Sorbonne Université, Université Pierre et Marie Curie (UPMC), Université de Paris 06, INSERM Unité 1127, Centre

National de la Recherche Scientifique (CNRS) Unité Mixte de Recherche 7225, Institut du Cerveau et de la Moelle Épinière (ICM), Paris 75013, France

c Université de Lille, Inserm, CHU-Lille, Alzheimer & Tauopathies, Lille, France

a

r

t

i

c

l

e

i

n

f

o

Article history: Received 18 May 2020 Accepted 18 June 2020 Available online 24 June 2020 Keywords:

Zebrafish (Danio Rerio) FUS KO model

Visual stimulation with the automatized viewpoint zebrabox system

Freezing response Behaviour

a

b

s

t

r

a

c

t

The data presented in this paper are related to the research article “Functional characterization of a FUS mutant zebrafish line as a novel genetic model for ALS”. In this model the lack of fus causes reduced lifespan as well as impaired motor abilities associated with a decrease of motor neurons axons lenght and an increase of neuromuscular junctions fragmen- tation.

Data in this article describes the global locomotor activity data at 3, 4 and 5 days post fertilization in WT, fus heterozy- gous (fus +/−) and fus homozygous (fus −/−) zebrafish embryos

as a response to visual light stimulation, with particular at- tention on the freezingrespose.

© 2020 Published by Elsevier Inc. This is an open access article under the CC BY-NC-ND license. ( http://creativecommons.org/licenses/by-nc-nd/4.0/)

DOI of original article: 10.1016/j.nbd.2020.104935

Corresponding author.

E-mail addresses: maria-letizia.campanari@institutimagine.org (M.-L. Campanari), edor.kabashi@institutimagine.org , edor.kabashi@icm-institute.org (E. Kabashi).

1 These authors contributed equally to this work.

https://doi.org/10.1016/j.dib.2020.105921

2352-3409/© 2020 Published by Elsevier Inc. This is an open access article under the CC BY-NC-ND license. ( http://creativecommons.org/licenses/by-nc-nd/4.0/ )

(3)

2 M.-L. Campanari, A.-R. Bourefis and V. Buee-Scherrer et al. / Data in Brief 31 (2020) 105921

Specifications

Table

Subject Neuroscience (General) Specific subject area Behavioural neuroscience Type of data Graph Figure

How data were acquired The aquisition was made with ZebraBox (Viewpoint Life Sciences, Lyon, France). Total swim activity was analysed using ZebraLab V3 software (Viewpoint Life Sciences, Lyon, France).

Data format Raw and Analyzed

Parameters for data collection 3 dpf-zebrafish larvae were maintained in a 96-well plate and assayed for total locomotor activity in ZebraBox. The embryos were tested for 10 min in a 5 min dark, 2 min light, 3 min dark paradigm, repeated 3 times. The experiment was done on the same fish at 4 and 5 dpf.

Description of data collection Tracking of zebrafish movements in an automated paradigm which uses light/darkness change as stimulus. In particular we looked at the behavior immediately after light stimulation, called freezing.

Data source location Imagine Institute, 75,015, Paris, France.

Data accessibility Data are supplied with this article Mendeley Dataset: campanari, Maria-Letizia (2020), “Freezing activity in a new FUS mutant zebrafish line ”, Mendeley Data, v1 http://dx.doi.org/10.17632/wyy6drwgwy.1

Related research article Annis-Rayan Bourefis, Maria-Letizia Campanari, Valerie Buee-Scherrer and Edor Kabashi . Functional characterization of a FUS mutant zebrafish line as a novel

genetic model for ALS. Neurobiology of disease. In press.

Value

of

the

Data

These

data

provides

a

protocol

for

locomotor

behavior

in

an

automatized

system

These

data

are

useful

for

those

interested

to

test

zebrafish

behavior

during

development.

These

results

provides

insights

about

zebrafish

locomotor

behavior

in

association

with

visual

system

development,

essential

for

zebrafish

survival.

It

can

be

applied

to

study

mutations

and/or

drug

treatments

important

for

locomotion.

The

advantage

of

this

technique

is

the

simultaneous

registration

of

the

peripheral

and

central

nervous

responses.

1.

Data

Description

Zebrafish

are

diurnal

animals,

meaning

that

they

are

particularly

active

during

light

ex-position

[1]

.

It

means

that

their

visual

system

is

refined

and

essential

for

their

proper

be-havior

development

and

survival

[2]

.

For

these

reasons

light

stimuli

tests

are

widely

used

in

(4)

Fig. 2. Freezing activity after light stimulation in WT, fus +/- and fus −/- embryos.

zebrafish

research

to

assess

their

motor

performances

independently

from

vision

defects

[2

,

3]

(

Figs.

1

and

2

).

For

each

light/darkness

condition

there

is

a

specific

swimming

behavior

response.

During

the

first

5

min

of

darkness

the

fish

adapts

to

its

condition,

it

is

quite

and

moves

randomly

in

the

well,

spontaneous

behavior

.

After

the

abrupt

stimulation

by

light

a

startle

response

appears

,

in

other

words

the

fish

reacts

to

light

with

a

strong

swimming

behavior.

The

increased

anxiety

brings

to

a

final

reduction

of

locomotion,

known

as

freezing

response,

which

is

characterized

by

(5)

4 M.-L. Campanari, A.-R. Bourefis and V. Buee-Scherrer et al. / Data in Brief 31 (2020) 105921

a

rapid

fall

of

activity

(

freezing

bouts

)

which

is

maintained

over

time

(

freezing

duration

).

Normally

it

is

followed

by

a

habituation

response,

where

anxiety

decreases

and

movements

are

reestab-lished.

In

[4]

we

determined

the

motor

impairment

in

a

new

model

for

FUS

loss

of

function

in

ze-brafish

respect

to

heterozygous

and

WT

fish,

at

3,

4

and

5

dpf

before

and

during

light

stimula-tion.

Here,

we

show

the

motor

behavior

during

the

freezing

response.

This

reaction

requires

spe-cific

areas

of

the

brain

(as

the

basolateral

amygdala

and

the

hippocampus).

Thus,

the

registration

of

this

behavior

confirms

the

presence

or

the

absence

of

developmental

defects

as

consequence

of

our

mutation

in

those

regions.

The

three

panels

are

quantifications

for

swimming

activity

during

freezing

bouts

and

duration

at

3,

4

and

5

dpf.

The

abrupt

stimulation

by

light

leads

to

a

startle

response

[4]

(

figure

3)

where

the

locomotion

activity

significantly

increases.

However,

this

behavior

is

followed

by

an

increase

of

the

anxiety

which

is

characterized

by

rapid

decrease

of

motor

activity

in

the

well

(freezing

bouts).

At

4dpf,

the

freezing

response

is

severely

compromised

in

fus

−/-

respect

to

heterozygous

and

WT

fish,

in

fact

it

still

move

(One-way

ANOVA

with

Bonferroni

post-hoc

test.

Freezing

bouts:

n

=

24,

36,

36;

F

=

4.10;

Freezing

duration:

n

=

24,

36,

36;

F

=

4.80.

p

<

0,

05).

However,

this

deficit

is

not

maintained

over

time,

as

we

can

see

at

5dpf.

To

have

more

information

about

the

global

locomotor

activity

at

each

periods

considered

during

our

protocol

in

WT,

fus

+/-

and

fus

−/-

embryos,

please

refer

to

the

article

[4]

,

figure

3,

C,

D,

E.

2.

Experimental

design,

materials,

and

methods

2.1.

Animal

care

Adult

and

larval

zebrafish

(Danio

rerio)

were

maintained

at

the

ICM

(Institut

du

Cerveau

et

de

la

Moelle

épinière,

Paris)

zebrafish

facility

and

bred

according

to

the

National

and

European

Guidelines

for

AnimalWelfare.

All

procedures

were

approved

by

the

Institutional

Ethics

Commit-tees

at

the

Research

Centers

of

ICM

and

Imagine.

Screening

of

mutant

lines:

refer

to

[4]

.

2.2.

Locomotion

assessment

3

dpf-zebrafish

larvae

were

maintained

in

a

96-well

plate

and

assayed

for

total

locomotor

activity

in

ZebraBox

(Viewpoint

Life

Sciences,

Lyon,

France).

The

embryos

were

tested

for

10

min

in

a

5

min

dark,

2

min

light

(100%),

3

min

dark

paradigm,

repeated

3

times.

The

experiment

was

done

on

the

same

fish

at

4

and

5

dpf.

Total

swim

activity

was

analysed

using

ZebraLab

V3

software

(Viewpoint

Life

Sciences,

Lyon,

France).

2.3.

Statistical

analysis

All

data

values

for

the

zebrafish

experiments

are

represented

as

average

standard

error

of

mean

(SEM)

with

significance

determined

using

one-way

ANOVAs.

Differences

between

groups

were

identified

via

post

hoc

comparisons,

specified

in

the

legend

of

the

Figure.

All

analyses

were

performed

using

Prism

5.0

(Graph

Pad,

CA).

Declaration

of

Competing

Interest

The

authors

declare

that

they

have

no

known

competing

financial

interests

or

personal

rela-tionships

which

have,

or

could

be

perceived

to

have,

influenced

the

work

reported

in

this

article.

(6)

Acknowledgment

This

project

was

supported

by

the

ERC

Consolidator

Grant,

AFM-Telethon

(EK)

and

the

Association

pour

la

Recherche

sur

la

Sclérose

Latérale

Amyotrophique

(ARSLA;

MLC

and

EK).

References

[1] R. Gerlai, M. Lahav, S. Guo, A. Rosenthal, Drinks like a fish: zebra fish (Danio Rerio) as a behavior genetic model to study alcohol effects, Pharmacol. Biochem. Behav. 67 (20 0 0) 773–782, doi: 10.1016/S0 091-3057(0 0)0 0422-6 . [2] S.C.F. Neuhauss, Behavioral genetic approaches to visual system development and function in zebrafish, J. Neurobiol.

54 (2003) 148–160, doi: 10.1002/neu.10165 .

[3] D.L. Champagne, C.C.M. Hoefnagels, R.E. De Kloet, M.K Richardson, Translating rodent behavioral repertoire to ze- brafish (Danio rerio): relevance for stress research, Behav. Brain Res. 214 (2010) 332–342, doi: 10.1016/j.bbr.2010.06. 001 .

[4] A.-.R. Bourefis , M.-.L. Campanari , V. Buee-Scherrer , E. Kabashi , Functional characterization of a FUS mutant zebrafish line as a novel genetic model for ALS, Neurobiol. Dis. (2020) In press .

Figure

Fig.  1. Automatized protocol used  at the Viewpoint Zebrabox  system  .
Fig.  2. Freezing activity  after light  stimulation in WT, fus  + /- and fus  −/- embryos

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