Literature DB >> 16439027

Breeding and maintenance of an Mecp2-deficient mouse model of Rett syndrome.

Denis G M Jugloff1, Richard Logan, James H Eubanks.   

Abstract

In this report, we present a retrospective assessment of our experiences in maintaining a colony of Mecp2-deficient mice, and present conditions that we have found to foster breeding success of this mutant mouse strain. Data from our colony of mutant Mecp2 mice show that the Mecp2-null allele is under-represented in the weaned litter population, that litters born to heterozygous Mecp2-null females are consistently smaller in number than wild-type, and that fewer litters from heterozygous Mecp2-null females survive to weaning age than wild-type. Our results also reveal that overall litter viability is significantly higher in heterozygous Mecp2-null females that frequently breed, and that the addition of sunflower seeds to the cages of expecting dams improves the overall breeding success of these mice. Taken together, these data highlight the breeding tendencies for this mutant mouse strain, and from these data, we suggest strategies to maximise their breeding efficiency.

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Year:  2006        PMID: 16439027     DOI: 10.1016/j.jneumeth.2005.12.002

Source DB:  PubMed          Journal:  J Neurosci Methods        ISSN: 0165-0270            Impact factor:   2.390


  9 in total

1.  Using environmental enrichment and nutritional supplementation to improve breeding success in rodents.

Authors:  Jaime Lecker; Karen Froberg-Fejko
Journal:  Lab Anim (NY)       Date:  2016-09-21       Impact factor: 12.625

2.  Early motor phenotype detection in a female mouse model of Rett syndrome is improved by cross-fostering.

Authors:  Annie Vogel Ciernia; Michael C Pride; Blythe Durbin-Johnson; Adriana Noronha; Alene Chang; Dag H Yasui; Jacqueline N Crawley; Janine M LaSalle
Journal:  Hum Mol Genet       Date:  2017-05-15       Impact factor: 6.150

3.  Mechanism of hyperphagia contributing to obesity in brain-derived neurotrophic factor knockout mice.

Authors:  E A Fox; J E Biddinger; K R Jones; J McAdams; A Worman
Journal:  Neuroscience       Date:  2012-10-13       Impact factor: 3.590

4.  Mecp2 deficiency decreases bone formation and reduces bone volume in a rodent model of Rett syndrome.

Authors:  R D O'Connor; M Zayzafoon; M C Farach-Carson; N C Schanen
Journal:  Bone       Date:  2009-05-03       Impact factor: 4.398

5.  Rett syndrome induced pluripotent stem cell-derived neurons reveal novel neurophysiological alterations.

Authors:  N Farra; W-B Zhang; P Pasceri; J H Eubanks; M W Salter; J Ellis
Journal:  Mol Psychiatry       Date:  2012-01-10       Impact factor: 15.992

6.  MeCP2 haplodeficiency and early-life stress interaction on anxiety-like behavior in adolescent female mice.

Authors:  María Abellán-Álvaro; Oliver Stork; Carmen Agustín-Pavón; Mónica Santos
Journal:  J Neurodev Disord       Date:  2021-12-11       Impact factor: 4.025

7.  Design of an improved set of oligonucleotide primers for genotyping MeCP2tm1.1Bird KO mice by PCR.

Authors:  Julie Miralvès; Eddy Magdeleine; Etienne Joly
Journal:  Mol Neurodegener       Date:  2007-08-31       Impact factor: 14.195

8.  Network models predict that reduced excitatory fluctuations can give rise to hippocampal network hyper-excitability in MeCP2-null mice.

Authors:  Ernest C Y Ho; James H Eubanks; Liang Zhang; Frances K Skinner
Journal:  PLoS One       Date:  2014-03-18       Impact factor: 3.240

9.  MeCP2 Related Studies Benefit from the Use of CD1 as Genetic Background.

Authors:  Clementina Cobolli Gigli; Linda Scaramuzza; Anna Gandaglia; Elisa Bellini; Marina Gabaglio; Daniela Parolaro; Charlotte Kilstrup-Nielsen; Nicoletta Landsberger; Francesco Bedogni
Journal:  PLoS One       Date:  2016-04-20       Impact factor: 3.240

  9 in total

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