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BAC transgenic mice express enhanced green fluorescent protein in central and peripheral cholinergic neurons.

BAC transgenic mice express enhanced green fluorescent protein in central and peripheral cholinergic neurons. Research Abstract Details 

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  • BAC transgenic mice express enhanced green fluorescent protein in central and peripheral cholinergic neurons. Abstract Text:

    yvonne n talliniYvonne N Tallini,bo shuiBo Shui,kai su greeneKai Su Greene,ke-yu dengKe-Yu Deng,robert doranRobert Doran,patricia j fisherPatricia J Fisher,warren zipfelWarren Zipfel,michael i kotlikoffMichael I Kotlikoff,

    The peripheral nervous system has complex and intricate ramifications throughout many target organ systems. To date this system has not been effectively labeled by genetic markers, due largely to inadequate transcriptional specification by minimum promoter constructs. Here we describe transgenic mice in which enhanced green fluorescent protein (eGFP) is expressed under the control of endogenous choline acetyltransferase (ChAT) transcriptional regulatory elements, by knock-in of eGFP within a bacterial artificial chromosome (BAC) spanning the ChAT locus and expression of this construct as a transgene. eGFP is expressed in ChAT(BAC)-eGFP mice in central and peripheral cholinergic neurons, including cell bodies and processes of the somatic motor, somatic sensory, and parasympathetic nervous system in gastrointestinal, respiratory, urogenital, cardiovascular, and other peripheral organ systems. Individual epithelial cells and a subset of lymphocytes within the gastrointestinal and airway mucosa are also labeled, indicating genetic evidence of acetylcholine biosynthesis. Central and peripheral neurons were observed as early as 10.5 days postcoitus in the developing mouse embryo. ChAT(BAC)-eGFP mice allow excellent visualization of all cholinergic elements of the peripheral nervous system, including the submucosal enteric plexus, preganglionic autonomic nerves, and skeletal, cardiac, and smooth muscle neuromuscular junctions. These mice should be useful for in vivo studies of cholinergic neurotransmission and neuromuscular coupling. Moreover, this genetic strategy allows the selective expression and conditional inactivation of genes of interest in cholinergic nerves of the central nervous system and peripheral nervous system.

    BAC transgenic mice express enhanced green fluorescent protein in central and peripheral cholinergic neurons. Publishing Authors By Initials

    yn talliniYN Tallini,b shuiB Shui,ks greeneKS Greene,ky dengKY Deng,r doranR Doran,pj fisherPJ Fisher,w zipfelW Zipfel,mi kotlikoffMI Kotlikoff,

    For similar nervous system: peripheral nervous system research abstracts see: nervous system: peripheral nervous system research

    PUBMED ID PMID:

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    BAC transgenic mice express enhanced green fluorescent protein in central and peripheral cholinergic neurons. Journal Published:

    PUBLICATION TYPE: Research Support, N.I.H., Extr

    Journal: Physiological genomics

    VOLUME: 27

    Page Numbers: 391-7

    Journal Abbreviation: Physiol. Genomics

    ISSN: 1531-2267

    DAY: 29

    MONTH: 08

    YEAR: 2006

    BAC transgenic mice express enhanced green fluorescent protein in central and peripheral cholinergic neurons. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 9815683

    BAC transgenic mice express enhanced green fluorescent protein in central and peripheral cholinergic neurons. Keywords Mesh Terms:

    KEYWORDS: Peripheral Nervous System

    MESH TERMS: metabolism

    Chemical & Substance for Abstract: BAC transgenic mice express enhanced green fluorescent protein in central and peripheral cholinergic neurons. Information

    Substance Name: Choline O-Acetyltransferase

    Registry Number: EC 2.3.1.6

    Grant and Affiliation Information for BAC transgenic mice express enhanced green fluorescent protein in central and peripheral cholinergic neurons.

    AFFILIATION: Biomedical Science Department, College of Veterinary Medicine, Ithaca, New York, USA.

    Country: United States

    United States Research PublicationUnited States Research Publication

    AGENCY: United States NHLBI

    GRANT: HL-76999

    ACRONYM: HL

    MEDLINETA: Physiol Genomics

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    DATABASENAME:

    ACCESSION NUMBER:

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