Imprinted Gene Expression and Function of the Dopa Decarboxylase Gene in the Developing Heart

被引:9
作者
Prickett, Adam R. [1 ]
Montibus, Bertille [1 ]
Barkas, Nikolaos [1 ,6 ]
Amante, Samuele M. [1 ,7 ]
Franco, Mauricio M. [1 ,8 ]
Cowley, Michael [1 ,9 ]
Puszyk, William [1 ]
Shannon, Matthew F. [1 ]
Irving, Melita D. [1 ,2 ]
Madon-Simon, Marta [3 ,4 ]
Ward, Andrew [3 ,4 ]
Schulz, Reiner [1 ]
Baldwin, H. Scott [5 ]
Oakey, Rebecca J. [1 ]
机构
[1] Kings Coll London, Dept Med & Mol Genet, London, England
[2] Guys & St Thomas NHS Fdn Trust, Dept Clin Genet, London, England
[3] Univ Bath, Dept Biol & Biochem, Bath, Avon, England
[4] Univ Bath, Ctr Regenerat Med, Bath, Avon, England
[5] Vanderbilt Univ, Med Ctr, Dept Pediat Cardiol, Nashville, TN USA
[6] Broad Inst, Human Cell Atlas Data Coordinat Platform, Data Sci Platform, Cambridge, MA USA
[7] Queen Mary Univ London, Barts & London Sch Med & Dent, Blizard Inst, Ctr Genom & Child Hlth, London, England
[8] Embrapa Genet Resources & Biotechnol, Lab Anim Reprod, Brasilia, DF, Brazil
[9] North Carolina State Univ, Ctr Human Hlth & Environm, Dept Biol Sci, Raleigh, NC USA
来源
FRONTIERS IN CELL AND DEVELOPMENTAL BIOLOGY | 2021年 / 9卷
基金
英国惠康基金; 美国国家卫生研究院; 英国医学研究理事会;
关键词
dopa decarboxylase; knock-out; imprinting; heart; mouse; human; ORIGIN ALLELIC EXPRESSION; GRB10; GENE; MOUSE; DISRUPTION; GROWTH; CELLS; MICE; RNA;
D O I
10.3389/fcell.2021.676543
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Dopa decarboxylase (DDC) synthesizes serotonin in the developing mouse heart where it is encoded by Ddc_exon1a, a tissue-specific paternally expressed imprinted gene. Ddc_exon1a shares an imprinting control region (ICR) with the imprinted, maternally expressed (outside of the central nervous system) Grb10 gene on mouse chromosome 11, but little else is known about the tissue-specific imprinted expression of Ddc_exon1a. Fluorescent immunostaining localizes DDC to the developing myocardium in the pre-natal mouse heart, in a region susceptible to abnormal development and implicated in congenital heart defects in human. Ddc_exon1a and Grb10 are not co-expressed in heart nor in brain where Grb10 is also paternally expressed, despite sharing an ICR, indicating they are mechanistically linked by their shared ICR but not by Grb10 gene expression. Evidence from a Ddc_exon1a gene knockout mouse model suggests that it mediates the growth of the developing myocardium and a thinning of the myocardium is observed in a small number of mutant mice examined, with changes in gene expression detected by microarray analysis. Comparative studies in the human developing heart reveal a paternal expression bias with polymorphic imprinting patterns between individual human hearts at DDC_EXON1a, a finding consistent with other imprinted genes in human.
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页数:10
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