首页> 外文期刊>Mechanisms of Ageing and Development >Telomeres shorten while Tert expression increases during ageing of the short-lived fish Nothobranchius furzeri.
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Telomeres shorten while Tert expression increases during ageing of the short-lived fish Nothobranchius furzeri.

机译:在短寿命鱼类Nothobranchius furzeri的衰老过程中,端粒缩短而Tert表达增加。

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摘要

Age research in vertebrates is often limited by the longevity of available models. The teleost fish Nothobranchius furzeri has an exceptionally short lifespan with 3.5 months for the laboratory strain GRZ and about 6 months for the wild-derived strain MZM-0403. Here we have investigated telomere length in muscle and skin tissue of young and old fish of both strains using different methods. We found age-dependent telomere shortening in the MZM-0403 strain with the longer lifespan, whereas the short-lived GRZ strain showed no significant telomere shortening with advanced age. Sequencing of the two main telomerase genes Tert and Terc revealed that both genes are highly conserved between the N. furzeri strains while there is little conservation to other fish species and humans. Both genes are ubiquitously expressed in N. furzeri and expression levels of Tert and Terc correlate with telomerase activity in a tissue-specific manner. Unexpectedly, the expression level of Tert is increased in aged muscle and skin tissue of MZM-0403 suggesting that telomeres shorten upon ageing despite increased Tert expression and hence high telomerase activity. We further conclude that the extremely short lifespan of the GRZ strain is not caused by diminished telomerase activity or accelerated telomere shortening.
机译:脊椎动物的年龄研究通常受到可用模型寿命的限制。硬骨鱼类Nothobranchius furzeri的寿命极短,实验室菌株GRZ的寿命为3.5个月,而野生菌株MZM-0403的寿命为约6个月。在这里,我们使用不同的方法研究了这两种菌株的幼鱼和老鱼的肌肉和皮肤组织中端粒的长度。我们发现寿命较长的MZM-0403菌株具有随年龄变化的端粒缩短,而寿命短的GRZ菌株随着年龄的增长没有明显的端粒缩短。两个主要的端粒酶基因Tert和Terc的测序表明,这两个基因在N. furzeri菌株之间是高度保守的,而对其他鱼类和人类则几乎没有保守性。两种基因都在糠N猪笼草中普遍表达,并且Tert和Terc的表达水平以组织特异性方式与端粒酶活性相关。出乎意料的是,MZM-0403的老化肌肉和皮肤组织中Tert的表达水平增加,这表明尽管Tert表达增加并因此端粒酶活性高,但端粒在老化时会缩短。我们进一步得出结论,GRZ菌株的极短寿命不是由端粒酶活性降低或端粒缩短缩短引起的。

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