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A phenotype survey of 36 mutant mouse strains with gene-targeted defects in glycosyltransferases or glycan-binding proteins

机译:表型调查了36个糖基转移酶或聚糖结合蛋白中基因靶向缺陷的突变小鼠品系

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摘要

The consortium for functional glycomics (CFG) was a large research initiative providing networking and resources for investigators studying the role of glycans and glycan-binding proteins in health and disease. Starting in 2001, six scientific cores were established to generate data, materials and new technologies. By the end of funding in 2011, the mouse phenotype core (MPC) submitted data to a website from the phenotype screen of 36 mutant mouse strains deficient in a gene for either a glycan-binding protein (GBP) or glycosyltransferase (GT). Each mutant strain was allotted three months for analysis and screened by standard phenotype assays used in the fields of immunology, histology, hematology, coagulation, serum chemistry, metabolism and behavior. Twenty of the deficient mouse strains had been studied in other laboratories, and additional tests were performed on these strains to confirm previous observations and discover new data. The CFG constructed 16 new homozygous mutant mouse strains and completed the initial phenotype screen of the majority of these new mutant strains. In total, >300 phenotype changes were observed, but considering the over 100 assays performed on each strain, most of the phenotypes were unchanged. Phenotype differences include abnormal testis morphology in GlcNAcT9- and Siglec-H-deficient mice and lethality in Pomgnt1-deficient mice. The numerous altered phenotypes discovered, along with the consideration of the significant findings of normality, will provide a platform for future characterization to understand the important roles of glycans and GBPs in the mechanisms of health and disease.
机译:功能糖组学联合会(CFG)是一项大型研究计划,为研究聚糖和聚糖结合蛋白在健康和疾病中的作用的研究人员提供了网络和资源。从2001年开始,建立了六个科学核心来生成数据,材料和新技术。到2011年资金末,小鼠表型核心(MPC)从表型筛选中向36个突变小鼠品系的网站提交了数据,这些突变体缺乏聚糖结合蛋白(GBP)或糖基转移酶(GT)的基因。每个突变株被分配三个月用于分析,并通过在免疫学,组织学,血液学,凝血,血清化学,代谢和行为领域中使用的标准表型测定法进行筛选。在其他实验室中已经研究了二十种缺陷小鼠品系,并对这些品系进行了额外的测试,以确认以前的观察结果并发现新的数据。 CFG构建了16个新的纯合突变小鼠品系,并完成了大多数这些新突变菌株的初始表型筛选。总体上,观察到> 300个表型变化,但是考虑到对每个菌株进行的100多次测定,大多数表型没有变化。表型差异包括GlcNAcT9和Siglec-H缺陷小鼠的睾丸形态异常和Pomgnt1缺陷小鼠的致死率。发现的众多改变的表型,以及对正常性重要发现的考虑,将为未来表征提供一个平台,以了解聚糖和GBP在健康和疾病机制中的重要作用。

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