Literature DB >> 18768146

Impaired recognition memory in male mice with a supernumerary X chromosome.

Lars Lewejohann1, Oliver S Damm, C Marc Luetjens, Tuula Hämäläinen, Manuela Simoni, Eberhard Nieschlag, Jörg Gromoll, Joachim Wistuba.   

Abstract

Several aberrant chromosomal constellations are known in men. Of these the karyotype XXY (Klinefelter syndrome, KS) is the most common chromosomal disorder with a prevalence of about one in 800 live-born boys. KS is associated with hypogonadism and is suspected to cause variable physical, physiological and cognitive abnormalities. As a supernumerary X chromosome is also associated with infertility, sound animal models for KS are difficult to obtain. In this study, male mice with two X chromosomes (XX(Y*)) were derived from fathers carrying a structurally rearranged Y chromosome (Y*) that resulted in physical attachment of a part of the Y chromosome to one X. These animals display certain physiological features that resemble closely those of human KS and can also be utilized to study X chromosomal imbalance and cognition. Therefore 15 XX(Y*) males and 15 XY* controls were subjected to a battery of behavioral tests, including a general health check, analysis of spontaneous exploration and locomotor activity, measures for anxiety-related behavior and the "novel object task" to test memory performance. Physiologically, XY* males did not differ from C57Bl/6 wild type mice carrying a normal Y chromosome, which provided a valid control group. All mice appeared healthy. XX(Y*) mice did not differ from their wild type littermates with respect to locomotion, exploration and anxiety-related behavior. XX(Y*) male mice, however, exhibited no significant recognition memory performance in contrast with wild type XY* males that readily fulfilled a given task. These findings support the hypothesis that the presence of a supernumerary X in male mice influences cognitive abilities. We suggest that the altered endocrine state and/or changes in the dosage of X-linked genes in the XX(Y*) mouse model affect brain function, in particular those regions responsible for cognition and learning behavior.

Entities:  

Mesh:

Substances:

Year:  2008        PMID: 18768146     DOI: 10.1016/j.physbeh.2008.08.007

Source DB:  PubMed          Journal:  Physiol Behav        ISSN: 0031-9384


  14 in total

Review 1.  Mouse model systems to study sex chromosome genes and behavior: relevance to humans.

Authors:  Kimberly H Cox; Paul J Bonthuis; Emilie F Rissman
Journal:  Front Neuroendocrinol       Date:  2014-01-02       Impact factor: 8.606

Review 2.  Consensus statement on diagnosis and clinical management of Klinefelter syndrome.

Authors:  A F Radicioni; A Ferlin; G Balercia; D Pasquali; L Vignozzi; M Maggi; C Foresta; A Lenzi
Journal:  J Endocrinol Invest       Date:  2010-12       Impact factor: 4.256

3.  Integrative DNA methylation and gene expression analysis identifies discoidin domain receptor 1 association with idiopathic nonobstructive azoospermia.

Authors:  Ranjith Ramasamy; Alex Ridgeway; Larry I Lipshultz; Dolores J Lamb
Journal:  Fertil Steril       Date:  2014-07-23       Impact factor: 7.329

4.  Feminized behavior and brain gene expression in a novel mouse model of Klinefelter Syndrome.

Authors:  Tuck C Ngun; Negar M Ghahramani; Michelle M Creek; Shayna M Williams-Burris; Hayk Barseghyan; Yuichiro Itoh; Francisco J Sánchez; Rebecca McClusky; Janet S Sinsheimer; Arthur P Arnold; Eric Vilain
Journal:  Arch Sex Behav       Date:  2014-06-13

Review 5.  Four Core Genotypes and XY* mouse models: Update on impact on SABV research.

Authors:  Arthur P Arnold
Journal:  Neurosci Biobehav Rev       Date:  2020-09-24       Impact factor: 8.989

6.  X-chromosome dosage affects male sexual behavior.

Authors:  Paul J Bonthuis; Kimberly H Cox; Emilie F Rissman
Journal:  Horm Behav       Date:  2012-02-10       Impact factor: 3.587

Review 7.  Sexual differentiation of brain and other tissues: Five questions for the next 50 years.

Authors:  Arthur P Arnold
Journal:  Horm Behav       Date:  2020-01-31       Impact factor: 3.587

Review 8.  Klinefelter syndrome: the commonest form of hypogonadism, but often overlooked or untreated.

Authors:  Eberhard Nieschlag
Journal:  Dtsch Arztebl Int       Date:  2013-05-17       Impact factor: 5.594

9.  Sexual differentiation in the developing mouse brain: contributions of sex chromosome genes.

Authors:  J T Wolstenholme; E F Rissman; S Bekiranov
Journal:  Genes Brain Behav       Date:  2013-01-10       Impact factor: 3.449

10.  Neural growth hormone implicated in body weight sex differences.

Authors:  Paul J Bonthuis; Emilie F Rissman
Journal:  Endocrinology       Date:  2013-07-16       Impact factor: 4.736

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.