1995
DOI: 10.1002/elps.11501601137
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A novel strategy to identify maternal and paternal inheritance in the mouse

Abstract: A novel strategy for identifying proteins which reveal maternal or paternal inheritance in the mouse is presented. Using two-dimensional electrophoresis we investigated protein expression patterns of adult liver and different embryonic and extraembryonic tissue in C57BL/6Crl and in DBA/2Crl mice, as well as in their reciprocal hybrids. We found three groups of protein spots which showed maternal or paternal inheritance of quantitative variations. These proteins were characterized by N-terminal or internal amin… Show more

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Cited by 6 publications
(3 citation statements)
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“…The present study is part of a long-term endeavor aimed at the identification of murine strain-specific protein variants, which reveal a mode of inheritance compatible with the concept of genomic imprinting, i.e., a maternal or paternal transmission [33,34]. Silver-stained 2-DE patterns of cytosolic liver proteins were investigated in 8 parental mice (2 mice of each gender) of the 2 subspecies M. musculus musculus (inbred strain: Calcinato B) and M. musculus domesticus (inbred strain: Aarhus) and in their offspring (25 F 1 hybrids: 14 females, 11 males).…”
Section: Resultsmentioning
confidence: 99%
“…The present study is part of a long-term endeavor aimed at the identification of murine strain-specific protein variants, which reveal a mode of inheritance compatible with the concept of genomic imprinting, i.e., a maternal or paternal transmission [33,34]. Silver-stained 2-DE patterns of cytosolic liver proteins were investigated in 8 parental mice (2 mice of each gender) of the 2 subspecies M. musculus musculus (inbred strain: Calcinato B) and M. musculus domesticus (inbred strain: Aarhus) and in their offspring (25 F 1 hybrids: 14 females, 11 males).…”
Section: Resultsmentioning
confidence: 99%
“…Proteins separated by 2-DE were blotted onto PVDF membranes (Millipore, Bedford, MA, USA), stained with Coomassie Brilliant Blue, and spots of interest were microsequenced and identified as described before [8,9]. Electrotransfer of the proteins on Hybond C nitrocellulose membranes (Amersham, Buckinghamshire, UK) was done under semidry blotting conditions [8] using the continous blotting buffer system described by Towbin et al [10] for both the covalent oxidative binding of DIG and the lectin affinoblotting. Glycoprotein staining was performed essentially following the standard procedure described by the manual of the DIG glycan detection kit (Boehringer, Mannheim, Germany).…”
mentioning
confidence: 99%
“…Glycoprotein staining was performed essentially following the standard procedure described by the manual of the DIG glycan detection kit (Boehringer, Mannheim, Germany). The procedure developed for blots of SDS-gels was adapted to 2-DE blots by repeating the blocking, washing, and incubation steps as previously published [8]. Dotblots of 0.5 mg bovine serum albumin and transferrin were used as positive controls, 0.5 mg deglycosylated creatinase as negative controls.…”
mentioning
confidence: 99%