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首页> 外文期刊>Marine biotechnology >Gene expression of a green fluorescent protein homolog as a host-specific biomarker of heat stress within a reef-building coral.
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Gene expression of a green fluorescent protein homolog as a host-specific biomarker of heat stress within a reef-building coral.

机译:绿色荧光蛋白同源物的基因表达,是珊瑚礁珊瑚内热应激的宿主特异性生物标志物。

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摘要

Recent incidences of mass coral bleaching indicate that major reef building corals are increasingly suffering thermal stress associated with climate-related temperature increases. The development of pulse amplitude modulated (PAM) fluorometry has enabled rapid detection of the onset of thermal stress within coral algal symbionts, but sensitive biomarkers of thermal stress specific to the host coral have been slower to emerge. Differential display reverse transcription polymerase chain reaction (DDRT-PCR) was used to produce fingerprints of gene expression for the reef-building coral Acropora millepora exposed to 33 degrees C. Changes in the expression of 23 out of 399 putative genes occurred within 144 h. Down-regulation of one host-specific gene (AmA1a) occurred within just 6 h. Full-length sequencing revealed the product of this gene to be an all-protein chromatophore (green fluorescent protein [GFP]-homolog). RT-PCR revealed consistent down-regulation of this GFP-homolog for three replicate colonies within 6 h at both 32 degrees C and 33 degrees C but not at lower temperatures. Down-regulation of this host gene preceded significant decreases in the photosynthetic activity of photosystem II (dark-adapted F (v)/F (m)) of algal symbionts as measured by PAM fluorometry. Gene expression of host-specific genes such as GFP-homologs may therefore prove to be highly sensitive indicators for the onset of thermal stress within host coral cells.
机译:最近发生的大规模珊瑚白化事件表明,主要的造礁珊瑚正日益遭受与气候相关的温度升高相关的热应力。脉冲幅度调制(PAM)荧光检测技术的发展已使快速检测珊瑚藻共生体内热应激的发生成为可能,但特定于宿主珊瑚的热应激敏感生物标志物的出现却较慢。差异显示逆转录聚合酶链反应(DDRT-PCR)用于产生暴露于33°C的珊瑚礁珊瑚Acropora millepora基因表达的指纹。399个推定基因中的23个表达的变化在144小时内发生。在短短6小时内,一个宿主特异性基因(AmA1a)的表达下调。全长测序表明该基因的产物是全蛋白色谱(绿色荧光蛋白[GFP]-同源物)。 RT-PCR显示在32℃和33℃下在6小时内,对于三个复制菌落,该GFP同源物一致下调,但在较低温度下没有。该宿主基因的下调先于藻类共生体的光系统II(暗适应的F(v)/ F(m))的光合作用的光合作用显着降低,如PAM荧光法所测。因此,宿主特异性基因(例如GFP同源基因)的基因表达可能是宿主珊瑚细胞内热应激发作的高度敏感指标。

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