LMX1B是一种LIM同源结构域类转录因子,是小鼠眼前段多个组织正常发育所必需的。

IF 1.5 4区 生物学 Q3 Biochemistry, Genetics and Molecular Biology
Genesis Pub Date : 2000-01-01
C L Pressman, H Chen, R L Johnson
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引用次数: 0

摘要

哺乳动物眼前段的正常发育对正常的眼功能至关重要。事实上,一些先天性综合征与前段异常可导致视力受损和青光眼。其中一种综合征是指甲髌骨综合征(NPS),由lim同源结构域转录因子LMX1B的单倍不足引起。虽然LMX1B突变与NPS共分离,但这些突变是否会导致NPS相关的青光眼尚不清楚。在这里,我们提供证据证明lim同源结构域转录因子lmx1b是小鼠前段发育的重要调节因子。靶突变lmx1b的纯合子小鼠表现为虹膜和睫状体发育不全,以及角膜基质缺陷。此外,在推定角膜中正常下调的两种cdna, mf1和mfh1,表现出持续表达,而角化细胞表达的硫酸角蛋白多糖,在突变角膜中未检测到。此外,纯合突变体的超微结构检查表明角膜胶原纤维形成受到干扰。综上所述,我们的研究提示了NPS患者青光眼的发育病因,并强调lmx1b是前段形态发生和模式的重要调节因子。创世纪26:15- 25,2000。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
LMX1B, a LIM homeodomain class transcription factor, is necessary for normal development of multiple tissues in the anterior segment of the murine eye.

Proper development of the anterior segment of the mammalian eye is critical for normal ocular function. Indeed, several congenital syndromes associated with anterior segment anomalies can lead to impaired vision and glaucoma. One such syndrome is nail patella syndrome (NPS), caused by haploinsufficiency for the LIM-homeodomain transcription factor LMX1B. Although mutations in LMX1B cosegregate with NPS, whether these mutations cause the glaucoma associated with NPS is not known. Here, we provide evidence that the LIM-homeodomain transcription factor lmx1b is an essential regulator of murine anterior segment development. Mice that are homozygous for a targeted mutation of lmx1b display iris and ciliary body hypoplasia, and cornea stromal defects. In addition, two cDNAs normally downregulated in presumptive cornea, mf1 and mfh1, exhibit persistent expression, while keratocan, a keratin sulfate proteoglycan expressed by keratocytes, is not detected in mutant corneas. Moreover, ultrastructural examination of homozygous mutants indicates that corneal collagen fibrillogenesis is perturbed. Taken together, our studies suggest a developmental etiology for glaucoma in NPS patients and highlight lmx1b as an essential regulator of anterior segment morphogenesis and patterning. genesis 26:15-25, 2000.

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来源期刊
Genesis
Genesis DEVELOPMENTAL BIOLOGY-GENETICS & HEREDITY
CiteScore
3.90
自引率
0.00%
发文量
19
期刊介绍: As of January 2000, Developmental Genetics was renamed and relaunched as genesis: The Journal of Genetics and Development, with a new scope and Editorial Board. The journal focuses on work that addresses the genetics of development and the fundamental mechanisms of embryological processes in animals and plants. With increased awareness of the interplay between genetics and evolutionary change, particularly during developmental processes, we encourage submission of manuscripts from all ecological niches. The expanded numbers of genomes for which sequencing is being completed will facilitate genetic and genomic examination of developmental issues, even if the model system does not fit the “classical genetic” mold. Therefore, we encourage submission of manuscripts from all species. Other areas of particular interest include: 1) the roles of epigenetics, microRNAs and environment on developmental processes; 2) genome-wide studies; 3) novel imaging techniques for the study of gene expression and cellular function; 4) comparative genetics and genomics and 5) animal models of human genetic and developmental disorders. genesis presents reviews, full research articles, short research letters, and state-of-the-art technology reports that promote an understanding of the function of genes and the roles they play in complex developmental processes.
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