Social and maternal behavior in mesoderm specific transcript (Mest)-deficient mice
Mesoderm specific transcript ( Mest )/paternally expressed gene-1 ( Peg1 ) is an imprinted gene expressed predominantly from the paternal allele. Aberrations in maternal behavior were previously reported in a Mest global knockout mouse ( Mest tm1Masu ). In this study, we performed in-depth social an...
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Published in: | PloS one 2022-07, Vol.17 (7), p.e0271913-e0271913 |
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Main Authors: | , , , |
Format: | Article |
Language: | eng |
Subjects: | |
Online Access: | Get full text |
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Summary: | Mesoderm specific transcript (
Mest
)/paternally expressed gene-1 (
Peg1
) is an imprinted gene expressed predominantly from the paternal allele. Aberrations in maternal behavior were previously reported in a
Mest
global knockout mouse (
Mest
tm1Masu
). In this study, we performed in-depth social and maternal behavioral testing in a mouse model of
Mest
inactivation developed in our laboratory (
Mest
tm1.2Rkz
). Mice with paternal allele inactivation (
Mest
pKO
) did not show anxiety after testing in the elevated plus maze, open field trial, and marble burying; nor depression-like behaviors in the tail suspension test.
Mest
pKO
showed normal social behaviors and memory/cognition in the three-chamber box test and the novel object recognition test, respectively. Primiparous
Mest
pKO
and
Mest
gKO
(biallelic
Mest
inactivation) female mice exhibited normal nest building and maternal behavior; and, virgin
Mest
pKO
and
Mest
gKO
female mice showed normal maternal instinct. Analyses of gene expression in adult hypothalamus, embryonic day 14.5 whole brain and adult whole brain demonstrated full abrogation of
Mest
mRNA in
Mest
pKO
and
Mest
gKO
mice with no effect on miR-335 expression. Our data indicates no discernible impairments in object recognition memory, social behavior or maternal behavior resulting from loss of
Mest
. The basis for the differences in maternal phenotypic behaviors between
Mest
tm1Masu
and
Mest
tm1.2Rkz
is not known. |
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ISSN: | 1932-6203 1932-6203 |