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1.
Bioinformatics ; 15(2): 170-1, 1999 Feb.
Article in English | MEDLINE | ID: mdl-10089202

ABSTRACT

SUMMARY: A single gene can generate multiple transcribed gene products. An extensive list of alternatively transcribed mouse genes has been generated, and is publicly available from http://www.informatics.jax.org/report.html. CONTACT: mgi-help@informatics.jax.org


Subject(s)
Alternative Splicing , Databases, Factual , Mice/genetics , Animals , Internet
2.
Nucleic Acids Res ; 27(1): 106-12, 1999 Jan 01.
Article in English | MEDLINE | ID: mdl-9847152

ABSTRACT

The Gene Expression Database (GXD) is a community resource that stores and integrates expression information for the laboratory mouse, with a particular emphasis on mouse development, and makes these data freely available in formats appropriate for comprehensive analysis. GXD is implemented as a relational database and integrated with the Mouse Genome Database (MGD) to enable global analysis of genotype, expression and phenotype information. Interconnections with sequence databases and with databases from other species further extend GXD's utility for the analysis of gene expression data. GXD is available through the Mouse Genome Informatics Web Site at http://www.informatics.jax.org/


Subject(s)
Databases, Factual , Gene Expression/genetics , Mice/genetics , Animals , Databases, Factual/trends , Expressed Sequence Tags , Genes , Genotype , Information Storage and Retrieval , Internet , Mice, Inbred Strains , Phenotype , Terminology as Topic
4.
Development ; 122(3): 771-81, 1996 Mar.
Article in English | MEDLINE | ID: mdl-8631255

ABSTRACT

Microtubule-associated protein 4 (MAP4) transcripts vary in different mouse tissues, with striated muscle (skeletal and cardiac) expressing 8- and 9-kb transcripts preferentially to the more widely distributed 5.5- and 6.5-kb transcripts (West, R. W., Tenbarge, K. M. and Olmsted, J. B. (1991). J. Biol. Chem. 266, 21886-21896). Cloning of the sequence unique to the muscle transcripts demonstrated that these mRNAs vary from the more ubiquitous ones by a single 3.2-kb coding region insertion within the projection domain of MAP4. During differentiation of the myogenic cell line, C2C12, muscle-specific MAP4 transcripts appear within 24 hours of growth in differentiation medium, and a larger MAP4 isotype (350 X 10(3) Mr) accumulates to high levels by 48 hours of differentiation. In situ hybridization analyses of transcript distribution in mouse embryos demonstrated that muscle-specific transcripts appear early in myogenesis. To block the expression of the muscle-specific MAP4, stable lines of C2C12 were generated bearing an antisense construct with the muscle-specific MAP4 sequence. Myoblast growth was unaffected whereas myotube formation was severely perturbed. Fusion occurred in the absence of the muscle MAP4 isotype, but the multinucleate syncytia were short and apolar, microtubules were disorganized and normal anisotropic myofibrils were absent. The patterns of expression of the muscle-specific transcripts and the antisense experiments indicated that this unique structural form of MAP4 plays a critical role in the formation and maintenance of muscle.


Subject(s)
Microtubule-Associated Proteins/genetics , Muscles/cytology , Amino Acid Sequence , Animals , Base Sequence , Cell Differentiation , Cells, Cultured , Fluorescent Antibody Technique, Indirect , Gene Expression Regulation, Developmental , In Situ Hybridization , Mice , Molecular Sequence Data , RNA, Messenger/genetics
5.
Exp Cell Res ; 199(2): 213-22, 1992 Apr.
Article in English | MEDLINE | ID: mdl-1544367

ABSTRACT

Although the presence of a matrix in plant nuclei has been reported, major questions remain about its structural and biochemical features. We have used an intermediate filament antibody of broad specificity to explore whether Daucus carota (carrot) nuclei and nuclear matrices contain intermediate filament/lamin antigens and, if so, where specifically they are localized. SDS-PAGE and Western blotting revealed two bands, at 60 and 65 kDa, that were highly immunoreactive with the intermediate filament antibody (IFA) of Pruss et al. (1981, Cell 27, 419-428). This pattern was observed consistently, not only with carrot cell-free nuclei and nuclear matrices, but also with nuclear preparations from Vicia faba (broad bean) and Pisum sativum (pea). Immunofluorescence studies with whole carrot nuclei localized the IFA antigens to the nucleoplasm and disclosed no accentuated peripheral labeling. Agarose-embedded nuclear matrices showed not only fluorescence throughout the nucleoplasm but also heavy labeling surrounding the nucleoli and suggestions of peripheral labeling. At the ultrastructural level, immunogold results from pre- and postembedment treatments supported the conclusion that IFA antigens occur throughout the nucleoplasm, with possibly a slight concentration at the periphery. These combined results provide substantial evidence that plant nuclei and their matrices possess at least two major intermediate filament antigens with molecular weights characteristic of animal lamins. Whether or not these antigens represent plant lamins, their nonperipheral localization hints at significant differences among the eukaryotic kingdoms in nuclear organization.


Subject(s)
Antigens/metabolism , Intermediate Filament Proteins/metabolism , Intermediate Filaments/immunology , Vegetables/metabolism , Blotting, Western , Cell Nucleus/immunology , Cell Nucleus/metabolism , Electrophoresis, Polyacrylamide Gel , Immunohistochemistry , Molecular Weight
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