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疏水性表面活性蛋白的遗传学

Genetics of the hydrophobic surfactant proteins.

作者信息

Nogee L M

机构信息

Division of Neonatology, Department of Pediatrics, Johns Hopkins University School of Medicine, Baltimore, MD, USA.

出版信息

Biochim Biophys Acta. 1998 Nov 19;1408(2-3):323-33. doi: 10.1016/s0925-4439(98)00078-7.

Abstract

The hydrophobic surfactant proteins, SP-B and SP-C, serve important roles in surfactant function and metabolism. Both proteins are encoded by single genes, located on human chromosomes 2 and 8 respectively, which have been characterized and extensively studied. Mutations in the SP-B gene have been shown to cause severe lung disease, and polymorphisms in the SP-B gene may be associated with the development of RDS in premature infants. In contrast, mutations in the SP-C gene have not yet been identified or shown to cause lung disease, although given the apparent importance of SP-C in surfactant function, this remains a possibility.

摘要

疏水性表面活性蛋白SP-B和SP-C在表面活性剂的功能和代谢中发挥着重要作用。这两种蛋白均由单基因编码,分别位于人类染色体2和8上,这些基因已得到表征并被广泛研究。研究表明,SP-B基因突变可导致严重的肺部疾病,且SP-B基因多态性可能与早产儿呼吸窘迫综合征的发生有关。相比之下,尽管SP-C在表面活性剂功能中显然很重要,但尚未发现SP-C基因突变或证实其会引发肺部疾病,不过这种可能性仍然存在。

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