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Localization of E2A mRNA expression in developing and adult rat tissues.

作者信息

Roberts V J, Steenbergen R, Murre C

机构信息

Department of Reproductive Medicine, University of California, San Diego, La Jolla 92093.

出版信息

Proc Natl Acad Sci U S A. 1993 Aug 15;90(16):7583-7. doi: 10.1073/pnas.90.16.7583.

DOI:10.1073/pnas.90.16.7583
PMID:8356060
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC47186/
Abstract

E2A helix-loop-helix proteins are involved in the control of various developmental pathways. We show here by in situ hybridization that E2A transcripts are present in most embryonic and adult tissues. However, no E2A expression is detectable in heart and nonproliferative regions of the brain and spinal cord. Highest levels of E2A expression are found in the ependyma cell layer surrounding the cerebral ventricles in the embryonic rat brain. In addition, in the embryo, E2A transcripts were found in secretory cells of the pancreas, the bronchial tubes of the lung, glomeruli of the kidney, and the lining of the stomach. Interestingly, high levels of E2A transcripts are selectively found in the germinal center of the lymphatic nodules in the adult rat spleen. Thus, E2A, like its Drosophila homolog daughterless, is expressed in most tissues. The most notable feature of the E2A expression pattern is its high levels of expression in some areas of rapid cell proliferation and differentiation and in certain epithelial cell types.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/baf0/47186/ecf3d67e3340/pnas01473-0171-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/baf0/47186/afd763204868/pnas01473-0169-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/baf0/47186/e29a835360dc/pnas01473-0169-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/baf0/47186/d64e6c8f0e5c/pnas01473-0170-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/baf0/47186/ecf3d67e3340/pnas01473-0171-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/baf0/47186/afd763204868/pnas01473-0169-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/baf0/47186/e29a835360dc/pnas01473-0169-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/baf0/47186/d64e6c8f0e5c/pnas01473-0170-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/baf0/47186/ecf3d67e3340/pnas01473-0171-a.jpg

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本文引用的文献

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A Novel Interaction between FLICE-Associated Huge Protein (FLASH) and E2A Regulates Cell Proliferation and Cellular Senescence via Tumor Necrosis Factor (TNF)-Alpha-p21WAF1/CIP1 Axis.FLICE相关巨蛋白(FLASH)与E2A之间的新型相互作用通过肿瘤坏死因子(TNF)-α-p21WAF1/CIP1轴调节细胞增殖和细胞衰老。
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