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无虹膜症:11p-染色体缺失的酶学研究

Aniridia: enzyme studies in an 11p--chromosomal deletion.

作者信息

Bateman J B, Sparkes M C, Sparkes R S

出版信息

Invest Ophthalmol Vis Sci. 1984 May;25(5):612-6.

PMID:6325367
Abstract

A patient with aniridia and an interstitial deletion of the bands p13-p14 of the short arm of chromosome 11 was studied to determine the relative locations of the gene(s) encoding for the aniridia-Wilms' tumor association with other genes on the same chromosome. Quantitative analysis was performed on the red blood cell enzymes lactic acid dehydrogenase-A (LDH-A) and catalase, the genes for which are located on the short arm of chromosome 11. The activity of LDH-A was normal; the activity of catalase was reduced to approximately half normal. This evidence supports loci for the genes encoding for both catalase and the aniridia-Wilms' tumor association within the bands p13-p14 of the short arm of chromosome 11; the normal activity of LDH-A supports a locus outside this region.

摘要

对一名患有无虹膜症且11号染色体短臂p13 - p14带间缺失的患者进行了研究,以确定与无虹膜 - 威尔姆斯瘤相关的基因在同一染色体上相对于其他基因的位置。对红细胞酶乳酸脱氢酶 - A(LDH - A)和过氧化氢酶进行了定量分析,其基因位于11号染色体短臂上。LDH - A的活性正常;过氧化氢酶的活性降至约正常水平的一半。这一证据支持了在11号染色体短臂p13 - p14带内存在编码过氧化氢酶和无虹膜 - 威尔姆斯瘤相关基因的位点;LDH - A的正常活性支持该区域外的一个位点。

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