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表达唾液酸特异性9-O-乙酰酯酶的转基因小鼠的发育异常。

Developmental abnormalities in transgenic mice expressing a sialic acid-specific 9-O-acetylesterase.

作者信息

Varki A, Hooshmand F, Diaz S, Varki N M, Hedrick S M

机构信息

Department of Medicine, University of California, San Diego 92093.

出版信息

Cell. 1991 Apr 5;65(1):65-74. doi: 10.1016/0092-8674(91)90408-q.

Abstract

9-O-acetylation of sialic acids is tissue specific and developmentally regulated. We have selectively destroyed these O-acetyl groups during murine embryogenesis by expressing the 9-O-acetyl-sialic acid-specific esterase of influenza C. DNA constructs driven by the metallothionein promoter arrested development at the 2-cell stage and gave a markedly decreased yield of live mice. A similar construct driven by the phenylethanolamine-N-methyltransferase promoter did not cause this block, but gave transgenic mice with selective expression of esterase in the retina and the adrenal gland. These organs showed variable abnormalities in organization, while all other tissues examined appeared normal. The ganglioside 9-O-acetyl-GD3 was selectively destroyed in target tissues. Thus, 9-O-acetylated sialic acids may play an role in murine development at the 2-cell stage and in certain differentiated tissues.

摘要

唾液酸的9-O-乙酰化具有组织特异性且受发育调控。我们通过表达丙型流感病毒的9-O-乙酰唾液酸特异性酯酶,在小鼠胚胎发生过程中选择性地破坏了这些O-乙酰基。由金属硫蛋白启动子驱动的DNA构建体使发育在2细胞阶段停滞,并导致活产小鼠的产量显著降低。由苯乙醇胺-N-甲基转移酶启动子驱动的类似构建体并未导致这种阻滞,但产生了在视网膜和肾上腺中选择性表达酯酶的转基因小鼠。这些器官在组织结构上表现出不同程度的异常,而所有其他检查的组织看起来正常。神经节苷脂9-O-乙酰-GD3在靶组织中被选择性破坏。因此,9-O-乙酰化唾液酸可能在小鼠2细胞阶段的发育以及某些分化组织中发挥作用。

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