Evidence of a bigenomic regulation of mitochondrial gene expression by thyroid hormone during rat brain development

被引:15
|
作者
Sinha, Rohit Anthony [1 ]
Pathak, Amrita [1 ]
Mohan, Vishwa [1 ]
Babu, Satish [1 ]
Pal, Amit [1 ]
Khare, Drirh [1 ]
Godbole, Madan M. [1 ]
机构
[1] Sanjay Gandhi Postgrad Inst Med Sci, Dept Endocrinol, Lucknow 226014, Uttar Pradesh, India
关键词
Thyroid hormone; Mitochondria; mTR; Brain development; Bigenomic; TRANSCRIPTION FACTOR; NUCLEAR; BIOGENESIS; HYPOTHYROIDISM; LOCALIZATION; RECEPTOR; COACTIVATOR; MORPHOLOGY; BINDING; MATRIX;
D O I
10.1016/j.bbrc.2010.05.154
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Hypothyroidism during early mammalian brain development is associated with decreased expression of various mitochondrial encoded genes along with evidence for mitochondrial dysfunction. However, inspite of the similarities between neurological disorders caused by perinatal hypothyroidism and those caused by various genetic mitochondrial defects we still do not know as to how thyroid hormone (TH) regulates mitochondrial transcription during development and whether this regulation by TH is nuclear mediated or through mitochondrial TH receptors? We here in rat cerebellum show that hypothyroidism causes reduction in expression of nuclear encoded genes controlling mitochondrial biogenesis like PGC-1 alpha, NRF-1 alpha and Tfam. Also, we for the first time demonstrate a mitochondrial localization of thyroid hormone receptor (mTR) isoform in developing brain capable of binding a TH response element (DR2) present in D-loop region of mitochondrial DNA. These results thus indicate an integrated nuclear-mitochondrial cross talk in regulation of mitochondrial transcription by TH during brain development. (C) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:548 / 552
页数:5
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