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BF-1基因缺陷小鼠眼睛的背腹模式形成缺陷与shh表达的局限性缺失相关。

Dorsal-ventral patterning defects in the eye of BF-1-deficient mice associated with a restricted loss of shh expression.

作者信息

Huh S, Hatini V, Marcus R C, Li S C, Lai E

机构信息

Cell Biology Program, Memorial Sloan-Kettering Cancer Center, New York, New York, 10021, USA.

出版信息

Dev Biol. 1999 Jul 1;211(1):53-63. doi: 10.1006/dbio.1999.9303.

Abstract

Brain factor 1 (BF-1) is a winged-helix transcription factor with restricted expression in the anterior optic vesicle and in the telencephalic neuroepithelium of the neural tube. We have previously found that targeted disruption of the BF-1 gene results in hypoplasia of the cerebral hemispheres, which is more severe in structures derived from the ventral telencephalon. Here we show that the loss of BF-1 leads to multiple developmental anomalies of the eyes. The most ventral structure arising from the optic vesicle, the optic stalk, is missing and is replaced by an expanded retina. Ventral closure of the optic cup and choroid fissure does not occur. These dorsal-ventral patterning defects are not limited to the BF-1-expressing (anterior) cells, but also involve the cells of the posterior optic vesicle. Sonic hedgehog (shh) expression within the ventral telencephalic neuroepithelium is specifically lost in the BF-1(-/-) mutant. Taken together, these findings suggest that shh produced at this site plays a role in patterning the developing eye. This localized deficit in shh expression may also contribute to the prominence of the ventral defects in the telencephalon of the BF-1(-/-) mutant.

摘要

脑因子1(BF-1)是一种翼状螺旋转录因子,在神经管的前视泡和端脑神经上皮中表达受限。我们之前发现,BF-1基因的靶向破坏会导致大脑半球发育不全,在源自腹侧端脑的结构中更为严重。在此我们表明,BF-1的缺失会导致眼睛出现多种发育异常。视泡产生的最腹侧结构——视神经柄缺失,取而代之的是扩张的视网膜。视杯和脉络膜裂的腹侧闭合未发生。这些背腹模式缺陷不仅限于表达BF-1的(前部)细胞,还涉及后视泡的细胞。腹侧端脑神经上皮内的音猬因子(shh)表达在BF-1(-/-)突变体中特异性缺失。综上所述,这些发现表明该部位产生的shh在发育中的眼睛模式形成中起作用。shh表达的这种局部缺陷也可能导致BF-1(-/-)突变体端脑腹侧缺陷的突出。

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