Sema3d and Sema7a Have Distinct Expression Patterns in Chick Embryonic Development.
From: Department of Medicine and Cell Biology, University of Massachusetts Medical School, Worcester, Massachusetts 02115, USA. zheng.bao@umassmed.edu
Developmental dynamics : an official publication of the American Association of Anatomists
- Publish Date: Aug 2006
- ISSN: 1058-8388
- Volume: 235
- Issue: 8
- Pages: 2282-9
- Medium: Print
- Language: English
- Citation (JAMA): Bao Zheng-Zheng, Jin Zhe, et al. Sema3d and Sema7a Have Distinct Expression Patterns in Chick Embryonic Development.. Dev. Dyn. Aug 2006;235:2282-9
Abstract
By RT-PCR, we isolated a partial cDNA clone for the chick Semaphorin7A (Sema7A) gene. We further analyzed its expression patterns and compared them with those of the Sema3D gene, in chick embryonic development. Sema3D and Sema7A appeared to be expressed in distinct cell populations. In mesoderm-derived structures, Sema7A expression was detected in the newly formed somites, whereas Sema3D expression was found in the notochord. In ectoderm-derived tissues, Sema3D is expressed broadly in the surface ectoderm, lens and nasal placodes. Sema3D is also expressed in the developing nervous system including diencephalon, dorsal neural tube, optical and otic vesicles. In the limb bud, Sema3D expression was found throughout the ectoderm excluding the apical ectoderm ridge (AER), where Sema7A is concentrated. Although both genes appeared to be expressed in the migrating neural crest cells, Sema3D expression is limited to neural crest cells migrating out of the midbrain/hindbrain regions, while Sema7A expression is widespread in both cranial and trunk neural crest cells.
Mesh Headings (Keywords): Amino Acid Sequence, Animals, Base Sequence, Chick Embryo, Cloning, Molecular, DNA, Complementary, Embryo, Nonmammalian, Gene Expression Regulation, Developmental, Humans, Molecular Sequence Data, Semaphorins, Sequence Alignment, Sequence Homology, Amino Acid, Time Factors, Transcription, Genetic
Check for Full Text / PubMed Unique Identifier (PMID): 16804892
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