Isolation of novel tissue-specific genes from cDNA libraries representing the individual tissue constituents of the gastrulating mouse embryo
Abstract
A total of 5 conventional, directionally cloned plasmid cDNA libraries have been constructed from the entire embryonic region of the mid-gastrulation mouse embryo and from its four principal tissue constituents (ectoderm, mesoderm, endoderm and primitive streak). These libraries have been validated with respect to the number of independent clones, insert-size and appropriate representation of diagnostic marker genes. Subtractive hybridisation has been used to remove clones common to the Endoderm and Mesoderm cDNA libraries resulting in an Endoderm minus Mesoderm subtracted library. Probe prepared from this subtracted library has been hybridised to a grid containing approximately 18,500 Embryonic Region library clones. Three novel clones have been recovered as well as expected genes already known to be highly expressed in the primitive endoderm lineage at this stage of development. In situ hybridisation to early postim-plantation embryos has revealed the expression patterns of these novel genes. One is highly expressed exclusively in visceral endoderm, one is expressed in ectodermal and endodermal tissues, and the third proves to be an early marker of prospective and differentiated surface ectoderm as well as being expressed in endoderm and its derivatives.
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Sousa-Nunes et al. identified 29/160 (18%) genes with restricted expression patterns from E7.5 mouse endoderm cDNA libraries using non-redundant sequence-based selection and in situ hybridization, but not all were endoderm enriched.
“Sousa-Nunes et al. identified 29/160 (18%) genes with restricted expression patterns from E7.5 mouse endoderm cDNA libraries using non-redundant sequence-based selection and in situ hybridization, but not all of these genes were endoderm enriched in their expression [40,41].”
From A systematic screen for genes expressed in definitive endoderm by Serial Analysis of Gene Expression (SAGE) (2007) · cites this paper as [41]
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- Authors
- Harrison, S. M., Dunwoodie, S. L., Arkell, R. M., Lehrach, H., & Beddington, R. S. P.
- Affiliations
- National Institute for Medical Research (GB)
- Max Planck Institute for Molecular Genetics (DE)
- Venue
- Development
- Publisher
- The Company of Biologists
- Published
- 1995-08-01
- Volume
- 121
- Issue
- 8
- Pages
- 2479-2489
- ISSN
- 0950-1991 (ISSN-L)
- 1477-9129
- OpenAlex
- W2105991972
- Cited by
- 71
- References
- 0
- Citations by year
- 2024: 3 · 2023: 3 · 2022: 1 · 2021: 1 · 2020: 2 · 2019: 2 · 2018: 1 · 2017: 1 · 2016: 1 · 2015: 2 · 2012: 1
- FWCI
- 1.97
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Development (publishedVersion)
- PubMed (publishedVersion)
- HighWire Press Open Archive (submittedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Developmental Biology and Gene Regulation
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Pluripotent Stem Cells Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Renal and related cancers
- Keywords
- tissue-specific genes, mouse embryo, gastrulation, cDNA library, endoderm, mesoderm, ectoderm, primitive streak, visceral endoderm, surface ectoderm, gene expression patterns, embryonic development, novel genes
- MeSH terms
- Animals, Base Sequence, Cloning, Molecular, Ectoderm, Endoderm, Gastrula, Mesoderm, Mice, Inbred C57BL, Mice, Inbred DBA, Molecular Sequence Data, Plasmids, Blotting, Southern, Gene Library, Gene Expression, In Situ Hybridization, DNA, Complementary, Mice
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