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首页> 外文期刊>Molecular biology reports >Alternative splicing generates a novel FADS2 alternative transcript in baboons
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Alternative splicing generates a novel FADS2 alternative transcript in baboons

机译:替代剪接在狒狒中产生新的FADS2替代转录本

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The mammalian fatty acid desaturase 2 (FADS2) gene codes for catalytic activity considered to be the rate limited step in long chain polyunsaturated fatty acid (LCPUFA) synthesis. FADS2 catalyzes 6-desaturation in at least five substrates and 8-desaturation in at least two substrates. However, the molecular mechanisms that regulate FADS2-mediated desaturation remain ill-defined. We report here characterization of an alternative transcript (AT1) of primate FADS2 and compare its expression to that of the classical transcript in 12 tissues of a 12 week old neonate baboon, and in human SK-N-SH neuroblastoma (NB) cells. RT-PCR analysis indicates relatively greater abundance of classical transcript than AT1 in all tissues. However, AT1 expression is highly variable, showing greater expression in liver, retina, occipital lobe, hippocampus, spleen, and ovary, than in other tissues, whereas classical transcript displayed little variability. These data suggest that FADS2 AT1 is a candidate for regulation of LCPUFA synthesis.
机译:哺乳动物脂肪酸去饱和酶2(FADS2)基因编码的催化活性被认为是长链多不饱和脂肪酸(LCPUFA)合成中的限速步骤。 FADS2在至少五个底物中催化6-去饱和,在至少两个底物中催化8-去饱和。但是,调节FADS2介导的去饱和的分子机制仍然不清楚。我们在这里报告了灵长类动物FADS2的替代转录本(AT1)的表征,并将其与经典转录本在12周龄新生狒狒的12个组织中以及在人类SK-N-SH神经母细胞瘤(NB)细胞中的表达进行了比较。 RT-PCR分析表明,在所有组织中,经典转录本的含量均比AT1更高。但是,AT1表达是高度可变的,与其他组织相比,在肝脏,视网膜,枕叶,海马,脾脏和卵巢中的表达更高,而经典转录本的变异性很小。这些数据表明FADS2 AT1是调节LCPUFA合成的候选基因。

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