Genetic Dissection of X-Linked Interspecific Hybrid Placental Dysplasia in Congenic Mouse Strains

Interspecific hybridization in the genus Mus results in male sterility and X-linked placental dysplasia. We have generated several congenic laboratory mouse lines (Mus musculus) in which different parts of the maternal X chromosome were derived from M. spretus. A strict positive correlation between...

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Published inGenetics (Austin) Vol. 153; no. 1; pp. 383 - 390
Main Authors Hemberger, Myriam C, Pearsall, Robert S, Zechner, Ulrich, Orth, Annie, Otto, Sabine, Ruschendorf, Franz, Fundele, Reinald, Elliott, Rosemary
Format Journal Article
LanguageEnglish
Published United States Genetics Soc America 01.09.1999
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Abstract Interspecific hybridization in the genus Mus results in male sterility and X-linked placental dysplasia. We have generated several congenic laboratory mouse lines (Mus musculus) in which different parts of the maternal X chromosome were derived from M. spretus. A strict positive correlation between placental weight and length of the M. spretus-derived part of the X chromosome was shown. Detailed analysis was carried out with one congenic strain that retained a M. spretus interval between 12.0 and 30.74 cM. This strain consistently produced hyperplastic placentas that exhibited an average weight increase of 180% over the weight of control placentas. In derived subcongenic strains, however, increased placental weight could no longer be observed. Morphometric analysis of these placentas revealed persistence of abnormal morphology. Fully developed placental hyperplasia could be reconstituted by recombination of proximal and central M. spretus intervals with an intervening M. musculus region. These results may suggest that placental dysplasia of interspecific mouse hybrids is caused by multiple loci clustered on the X chromosome that act synergistically. Alternatively, it is possible that changes in chromatin structure in interspecific hybrids that influence gene expression are dependent on the length of the alien chromosome.
AbstractList Abstract Interspecific hybridization in the genus Mus results in male sterility and X-linked placental dysplasia. We have generated several congenic laboratory mouse lines (Mus musculus) in which different parts of the maternal X chromosome were derived from M. spretus. A strict positive correlation between placental weight and length of the M. spretus-derived part of the X chromosome was shown. Detailed analysis was carried out with one congenic strain that retained a M. spretus interval between 12.0 and 30.74 cM. This strain consistently produced hyperplastic placentas that exhibited an average weight increase of 180% over the weight of control placentas. In derived subcongenic strains, however, increased placental weight could no longer be observed. Morphometric analysis of these placentas revealed persistence of abnormal morphology. Fully developed placental hyperplasia could be reconstituted by recombination of proximal and central M. spretus intervals with an intervening M. musculus region. These results may suggest that placental dysplasia of interspecific mouse hybrids is caused by multiple loci clustered on the X chromosome that act synergistically. Alternatively, it is possible that changes in chromatin structure in interspecific hybrids that influence gene expression are dependent on the length of the alien chromosome.
Interspecific hybridization in the genus Mus results in male sterility and X-linked placental dysplasia. We have generated several congenic laboratory mouse lines (Mus musculus) in which different parts of the maternal X chromosome were derived from M. spretus. A strict positive correlation between placental weight and length of the M. spretus-derived part of the X chromosome was shown. Detailed analysis was carried out with one congenic strain that retained a M. spretus interval between 12.0 and 30.74 cM. This strain consistently produced hyperplastic placentas that exhibited an average weight increase of 180% over the weight of control placentas. In derived subcongenic strains, however, increased placental weight could no longer be observed. Morphometric analysis of these placentas revealed persistence of abnormal morphology. Fully developed placental hyperplasia could be reconstituted by recombination of proximal and central M. spretus intervals with an intervening M. musculus region. These results may suggest that placental dysplasia of interspecific mouse hybrids is caused by multiple loci clustered on the X chromosome that act synergistically. Alternatively, it is possible that changes in chromatin structure in interspecific hybrids that influence gene expression are dependent on the length of the alien chromosome.
Author Zechner, Ulrich
Elliott, Rosemary
Pearsall, Robert S
Otto, Sabine
Fundele, Reinald
Orth, Annie
Ruschendorf, Franz
Hemberger, Myriam C
AuthorAffiliation Max-Planck-Institut für Molekulare Genetik, 14195 Berlin, Germany
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Snippet Interspecific hybridization in the genus Mus results in male sterility and X-linked placental dysplasia. We have generated several congenic laboratory mouse...
Abstract Interspecific hybridization in the genus Mus results in male sterility and X-linked placental dysplasia. We have generated several congenic laboratory...
Interspecific hybridization in the genus Mus results in male sterility and X- linked placental dysplasia. We have generated several congenic laboratory mouse...
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StartPage 383
SubjectTerms Animals
Crosses, Genetic
Female
Fetus - abnormalities
Gene Expression
Genetic Linkage - genetics
Genetic Markers - genetics
Genotype
Haplotypes - genetics
Male
Mice
Mice, Congenic
Mice, Inbred C3H
Mice, Inbred C57BL
Mus musculus
Mus spretus
Organ Size
Phenotype
Placenta - abnormalities
Placenta - embryology
Placenta - pathology
Pregnancy
X Chromosome - genetics
Title Genetic Dissection of X-Linked Interspecific Hybrid Placental Dysplasia in Congenic Mouse Strains
URI http://www.genetics.org/cgi/content/abstract/153/1/383
https://www.ncbi.nlm.nih.gov/pubmed/10471720
https://search.proquest.com/docview/17322070
https://search.proquest.com/docview/70011772
https://pubmed.ncbi.nlm.nih.gov/PMC1460747
Volume 153
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