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脑特异性原肌球蛋白TMBr-1和TMBr-3在发育过程和成年大脑中具有不同的表达模式。

Brain-specific tropomyosins TMBr-1 and TMBr-3 have distinct patterns of expression during development and in adult brain.

作者信息

Stamm S, Casper D, Lees-Miller J P, Helfman D M

机构信息

Cold Spring Harbor Laboratory, NY 11724.

出版信息

Proc Natl Acad Sci U S A. 1993 Nov 1;90(21):9857-61. doi: 10.1073/pnas.90.21.9857.

DOI:10.1073/pnas.90.21.9857
PMID:7694294
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC47671/
Abstract

In this study we report on the developmental and regional expression of two brain-specific isoforms of tropomyosin, TMBr-1 and TMBr-3, that are generated from the rat alpha-tropomyosin gene via the use of alternative promoters and alternative RNA splicing. Western blot analysis using an exon-specific peptide polyclonal antibody revealed that the two isoforms are differentially expressed in development with TMBr-3 appearing in the embryonic brain at 16 days of gestation, followed by the expression of TMBr-1 at 20 days after birth. TMBr-3 was detected in all brain regions examined, whereas TMBr-1 was detected predominantly in brain areas that derived from the prosencephalon. Immunocytochemical studies on mixed primary cultures made from rat embryonic midbrain indicate that expression of the brain-specific epitope is restricted to neurons. The developmental pattern and neuronal localization of these forms of tropomyosin suggest that these isoforms have a specialized role in the development and plasticity of the nervous system.

摘要

在本研究中,我们报告了原肌球蛋白的两种脑特异性同工型TMBr-1和TMBr-3的发育及区域表达情况,它们是通过使用不同的启动子和选择性RNA剪接从大鼠α-原肌球蛋白基因产生的。使用外显子特异性肽多克隆抗体进行的蛋白质印迹分析表明,这两种同工型在发育过程中差异表达,TMBr-3在妊娠16天时出现在胚胎脑中,随后在出生后20天时表达TMBr-1。在所检查的所有脑区中均检测到TMBr-3,而TMBr-1主要在源自前脑的脑区中检测到。对大鼠胚胎中脑混合原代培养物进行的免疫细胞化学研究表明,脑特异性表位的表达仅限于神经元。这些原肌球蛋白形式的发育模式和神经元定位表明,这些同工型在神经系统的发育和可塑性中具有特殊作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e7f/47671/fa25d7aa0f1e/pnas01528-0131-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e7f/47671/0c4e8ffe9a45/pnas01528-0128-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e7f/47671/714494393703/pnas01528-0128-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e7f/47671/25e8baf6c6f9/pnas01528-0129-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e7f/47671/bfe5ecc31137/pnas01528-0129-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e7f/47671/7801d7ef2ef8/pnas01528-0130-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e7f/47671/fa25d7aa0f1e/pnas01528-0131-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e7f/47671/0c4e8ffe9a45/pnas01528-0128-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e7f/47671/714494393703/pnas01528-0128-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e7f/47671/25e8baf6c6f9/pnas01528-0129-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e7f/47671/bfe5ecc31137/pnas01528-0129-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e7f/47671/7801d7ef2ef8/pnas01528-0130-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e7f/47671/fa25d7aa0f1e/pnas01528-0131-a.jpg

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J Cell Biol. 1993 Jan;120(1):205-15. doi: 10.1083/jcb.120.1.205.
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