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一种绿色荧光蛋白同源物的基因表达作为造礁珊瑚内热应激的宿主特异性生物标志物。

Gene expression of a green fluorescent protein homolog as a host-specific biomarker of heat stress within a reef-building coral.

作者信息

Smith-Keune C, Dove S

机构信息

Centre for Marine Studies, ARC Centre of Excellence for Coral Reef Studies, University of Queensland, St Lucia, Queensland 4072, Australia.

出版信息

Mar Biotechnol (NY). 2008 Mar-Apr;10(2):166-80. doi: 10.1007/s10126-007-9049-6. Epub 2007 Nov 11.

Abstract

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.

摘要

近期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所带来的热应激。脉冲幅度调制(PAM)荧光测定法的发展使得能够快速检测珊瑚藻共生体中热应激的开始,但针对宿主珊瑚的热应激敏感生物标志物的出现则较为缓慢。采用差异显示逆转录聚合酶链反应(DDRT-PCR)来生成暴露于33摄氏度的造礁珊瑚多孔鹿角珊瑚的基因表达指纹图谱。在399个推定基因中,有23个基因的表达在144小时内发生了变化。其中一个宿主特异性基因(AmA1a)在仅6小时内就出现了下调。全长测序显示该基因的产物是一种全蛋白色素细胞(绿色荧光蛋白[GFP]同源物)。逆转录聚合酶链反应(RT-PCR)显示,在32摄氏度和33摄氏度下,三个重复菌落中的这种GFP同源物在6小时内均出现了一致的下调,但在较低温度下则未出现。通过PAM荧光测定法测量,该宿主基因的下调先于藻共生体光系统II的光合活性(暗适应F(v)/F(m))显著下降。因此,宿主特异性基因如GFP同源物的基因表达可能被证明是宿主珊瑚细胞内热应激开始的高度敏感指标。

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