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神经酰胺激酶样蛋白在小鼠视网膜中的时空表达模式

Spatiotemporal expression pattern of ceramide kinase-like in the mouse retina.

作者信息

Vekslin Sharon, Ben-Yosef Tamar

机构信息

Department of Genetics, Rappaport Faculty of Medicine, Technion-Israel Institute of Technology, Haifa, Israel.

出版信息

Mol Vis. 2010 Dec 3;16:2539-49.

Abstract

PURPOSE

The CERKL gene encodes for ceramide kinase-like, a novel protein of unknown function. CERKL mutations are associated with a severe retinal phenotype. The purpose of this work was to investigate alternative splicing, and the temporal and spatial expression pattern of CERKL in the mouse retina.

METHODS

Reverse Transcription-Polymerase Chain Reaction (RT-PCR) analysis of mouse retina RNA was used to study the expression of Cerkl at various developmental time points, and to identify its various splice-isoforms. A specific anti-CERKL antibody was developed and used for immunostaining to study the localization of the endogenous CERKL protein in retina-derived cell lines and in the mouse retina.

RESULTS

Cerkl is expressed in the mouse eye as early as embryonic day 14. A total of seven different Cerkl splice-isoforms were identified in the mouse retina. The subcellular localization of CERKL in retina-derived cell lines is variable: CERKL is diffusely distributed in the cytoplasm, and in many cells, it is highly concentrated in the perinuclear region. In most, but not all cells, CERKL is also highly concentrated in the nucleus. In the mouse retina, CERKL is located in the ganglion cell layer, in amacrine cells of the inner nuclear layer, and in photoreceptors. CERKL is highly expressed in cone photoreceptors; however, its expression level in rod photoreceptors is very low. In cultured cells, CERKL is detected in the nucleus, but in retinal cells in situ, it is mostly located in the cytoplasm.

CONCLUSIONS

The expression of Cerkl in both mature and embryonic mouse retina and the severe retinal phenotype associated with human CERKL mutations indicate that this gene plays a crucial role in retinal activity, and that it may be important for retinal development as well. The high expression level of CERKL in cones correlates with the CERKL-associated phenotype in humans. Whether nucleocytoplasmic transport of CERKL actually occurs in vivo under certain conditions and its functional significance remain to be discovered.

摘要

目的

CERKL基因编码神经酰胺激酶样蛋白,这是一种功能未知的新型蛋白质。CERKL突变与严重的视网膜表型相关。本研究的目的是调查小鼠视网膜中CERKL的可变剪接以及时空表达模式。

方法

采用逆转录-聚合酶链反应(RT-PCR)分析小鼠视网膜RNA,以研究Cerkl在不同发育时间点的表达,并鉴定其各种剪接异构体。开发了一种特异性抗CERKL抗体,并用于免疫染色,以研究内源性CERKL蛋白在视网膜衍生细胞系和小鼠视网膜中的定位。

结果

Cerkl早在胚胎第14天就在小鼠眼中表达。在小鼠视网膜中总共鉴定出七种不同的Cerkl剪接异构体。CERKL在视网膜衍生细胞系中的亚细胞定位是可变的:CERKL在细胞质中呈弥散分布,在许多细胞中,它高度集中在核周区域。在大多数但不是所有细胞中,CERKL也高度集中在细胞核中。在小鼠视网膜中,CERKL位于神经节细胞层、内核层的无长突细胞和光感受器中。CERKL在视锥光感受器中高度表达;然而,其在视杆光感受器中的表达水平非常低。在培养细胞中,CERKL在细胞核中被检测到,但在原位视网膜细胞中,它大多位于细胞质中。

结论

Cerkl在成熟和胚胎小鼠视网膜中的表达以及与人类CERKL突变相关的严重视网膜表型表明,该基因在视网膜活动中起关键作用,并且对视网膜发育可能也很重要。CERKL在视锥细胞中的高表达水平与人类CERKL相关表型相关。CERKL在体内是否在某些条件下实际发生核质运输及其功能意义仍有待发现。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/61a2/3000240/6d29b91db583/mv-v16-2539-f1.jpg

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