Yang Kun, Zhou Xiao-nong, Yu Chuan-xin, Yin Xu-ren, Hong Qing-biao, Sun Le-ping, Yang Guo-jing, Zhang Yan-ping, Huang Yi-xin
Jiangsu Institute of Parasitic Diseases, Wuxi 214064.
Zhongguo Ji Sheng Chong Xue Yu Ji Sheng Chong Bing Za Zhi. 2003;21(3):140-3.
To study the expression of nitric oxide synthase (NOS) mRNA in the gonad of Oncomelania hupensis in different temperature.
The snails were cultured at temperature of 0 degree C, 15 degrees C and 25 degrees C for 1 month. The total RNA of each group was extracted with the RNA extraction kit. A pair of degenerate primers was designed from conserved regions of mammalian NOSs, and the expression of NOS mRNA in the gonad was measured by means of reverse transcription polymerase chain reaction (RT-PCR).
The target genes of NOS were detected in the gonad of snails. The level of expression of snail NOS mRNA in 25 degrees C group and 0 degree C group was significantly higher than that in the control group(P < 0.01), there was no significant difference for the expression products between 15 degrees C group and control group (P > 0.05).
The designation of primers of the snails was validated. The impact of temperature on the expression of snail NOS mRNA was determined, which suggested that NO plays an important role in the physiological and pathological modulation.
研究不同温度下钉螺性腺中一氧化氮合酶(NOS)mRNA的表达情况。
将钉螺分别在0℃、15℃和25℃温度下培养1个月。用RNA提取试剂盒提取每组钉螺的总RNA。根据哺乳动物NOS的保守区设计一对简并引物,采用逆转录聚合酶链反应(RT-PCR)检测钉螺性腺中NOS mRNA的表达。
在钉螺性腺中检测到NOS的靶基因。25℃组和0℃组钉螺NOS mRNA的表达水平显著高于对照组(P<0.01),15℃组与对照组的表达产物无显著差异(P>0.05)。
验证了钉螺引物的设计。确定了温度对钉螺NOS mRNA表达的影响,提示一氧化氮在生理和病理调节中起重要作用。