Beutler E, Gelbart T, West C, Kuhl W, Lee P
Department of Molecular and Experimental Medicine, Scripps Research Institute, La Jolla, California, USA.
Blood Cells Mol Dis. 1995;21(3):207-16. doi: 10.1006/bcmd.1995.0024.
Selective hybridization of small intestine and liver cDNA libraries was carried out using yeast artificial chromosomes (YACs) surrounding D6S105, the microsatellite that appears to be close to the gene for hereditary hemochromatosis (HFE). Of 14 candidate probes hybridizing with these YACs, only one, designated. LD5-1, detected abnormalities in southern blots of patients with hemochromatosis. Two different abnormalities. were detected in 3 of 55 patients with hemochromatosis with the LD5-1 probe, and one of these was detected in one of 44 normal subjects. The gene that hybridizes with this probe is located about 300-400 kb centromeric of D6S105. It is transcribed into mRNA that is about 8.5 kb in length in many tissues, including peripheral blood leukocytes. The available sequence indicates tha it codes for a zinc finger protein. We propose that there is a reasonable probability that LD5-1 hybridizes with the gene for hereditary hemochromatosis.
使用围绕D6S105的酵母人工染色体(YAC)对小肠和肝脏cDNA文库进行了选择性杂交,D6S105是一个微卫星,似乎与遗传性血色素沉着症(HFE)基因接近。在与这些YAC杂交的14个候选探针中,只有一个命名为LD5-1的探针在血色素沉着症患者的Southern印迹中检测到异常。在55例血色素沉着症患者中,有3例用LD5-1探针检测到两种不同的异常,其中一种在44名正常受试者中的1名中检测到。与该探针杂交的基因位于D6S105着丝粒约300 - 400 kb处。它转录成的mRNA在包括外周血白细胞在内的许多组织中长度约为8.5 kb。现有的序列表明它编码一种锌指蛋白。我们认为LD5-1与遗传性血色素沉着症基因杂交有合理的可能性。