Fan Qiuling, Shike Toshihide, Shigihara Takako, Tanimoto Mitsuo, Gohda Tomohito, Makita Yuichiro, Wang Li Ning, Horikoshi Satoshi, Tomino Yasuhiko
Division of Nephrology, Department of Internal Medicine, Juntendo University School of Medicine, Tokyo, Japan.
Kidney Int. 2003 Dec;64(6):1978-85. doi: 10.1046/j.1523-1755.2003.00312.x.
To identify susceptibility genes for diabetic nephropathy, GeneChip Expression Analysis was employed to survey the gene expression profile of diabetic KK/Ta mouse kidneys.
Kidneys from three KK/Ta and two BALB/c mice at 20 weeks of age were dissected. Total RNA was extracted and labeled for hybridizing to the Affymetrix Murine Genome U74Av2 array. The gene expression profile was compared between KK/Ta and BALB/c mice using GeneChip expression analysis software. Competitive reverse transcription-polymerase chain reaction (RT-PCR) was used to confirm the results of GeneChip for a selected number of genes.
Out of 12,490 probe pairs present on GeneChip, 98 known genes and 31 expressed sequence tags (ESTs) were found to be differentially expressed between KK/Ta and BALB/c kidneys. Twenty-one known genes and seven ESTs that increased in expression and 77 known genes and 24 ESTs that decreased in KK/Ta kidneys were identified. These genes are related to renal function, extracellular matrix expansion and degradation, signal transduction, transcription regulation, ion transport, glucose and lipid metabolism, and protein synthesis and degradation. In the vicinity of UA-1 (quantitative trait locus for the development of albuminuria in KK/Ta mice), candidate genes that showed differential expression were identified, including the Sdc4 gene for syndecan-4, Ahcy gene for S-adenosylhomocysteine hydrolase, Sstr4 gene for somatostatin receptor 4, and MafB gene for Kreisler leucine zipper protein.
The gene expression profile in KK/Ta kidneys is different from that in age-matched BALB/c kidneys. Altered gene expressions in the vicinity of UA-1 may be responsible for the development of albuminuria in diabetic KK/Ta mice.
为了鉴定糖尿病肾病的易感基因,采用基因芯片表达分析技术检测糖尿病KK/Ta小鼠肾脏的基因表达谱。
解剖20周龄的3只KK/Ta小鼠和2只BALB/c小鼠的肾脏。提取总RNA并进行标记,用于与Affymetrix鼠基因组U74Av2芯片杂交。使用基因芯片表达分析软件比较KK/Ta小鼠和BALB/c小鼠之间的基因表达谱。采用竞争性逆转录-聚合酶链反应(RT-PCR)对选定的一些基因进行检测,以确认基因芯片的结果。
在基因芯片上的12490个探针组中,发现98个已知基因和31个表达序列标签(EST)在KK/Ta小鼠和BALB/c小鼠的肾脏中差异表达。鉴定出21个表达增加的已知基因和7个EST,以及77个表达减少的已知基因和24个EST。这些基因与肾功能、细胞外基质的扩张和降解、信号转导、转录调控、离子转运、葡萄糖和脂质代谢以及蛋白质合成和降解有关。在UA-1(KK/Ta小鼠蛋白尿发生的数量性状位点)附近,鉴定出了差异表达的候选基因,包括多配体蛋白聚糖-4的Sdc4基因、S-腺苷同型半胱氨酸水解酶的Ahcy基因、生长抑素受体4的Sstr4基因和克雷斯勒亮氨酸拉链蛋白的MafB基因。
KK/Ta小鼠肾脏的基因表达谱与年龄匹配的BALB/c小鼠不同。UA-1附近基因表达的改变可能是糖尿病KK/Ta小鼠蛋白尿发生的原因。