Natural melatonin 'knockdown' in C57BL/6J mice:: rare mechanism truncates serotonin N-acetyltransferase

被引:214
作者
Roseboom, PH
Namboodiri, MAA
Zimonjic, DB
Popescu, NC
Rodriguez, IR
Gastel, JA
Klein, DC
机构
[1] NICHHD, Sect Neuroendocrinol, Dev Neurobiol Lab, NIH, Bethesda, MD 20892 USA
[2] NCI, Expt Carcinogenesis Lab, NIH, Bethesda, MD 20892 USA
[3] NEI, Retinal Cell & Mol Biol Lab, NIH, Bethesda, MD 20892 USA
来源
MOLECULAR BRAIN RESEARCH | 1998年 / 63卷 / 01期
关键词
pineal; retina; C3H/HeJ; circadian; RNA splicing; cryptic splice acceptor site;
D O I
10.1016/S0169-328X(98)00273-3
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Pineal melatonin synthesis (serotonin --> N-acetylserotonin --> melatonin) is severely compromised in most inbred strains of mice, in many cases because serotonin is not acetylated by serotonin N-acetyltransferase (arylalkylamine N-acetyltransferase, AANAT). We have found that in the C57BL/6J strain, AANAT mRNA encodes a severely truncated AANAT protein, because a pseudo-exon containing a stop codon is spliced in. This is the first identification of a natural mutation which knocks down melatonin synthesis. The decrease in melatonin signaling may have been a selective factor in the development of laboratory strains of mice because melatonin can inhibit reproduction and modify circadian rhythmicity. (C) 1998 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:189 / 197
页数:9
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