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斑马鱼sox9突变体的表达谱分析表明,视网膜分化需要Sox9。

Expression profiling of zebrafish sox9 mutants reveals that Sox9 is required for retinal differentiation.

作者信息

Yokoi Hayato, Yan Yi-Lin, Miller Michael R, BreMiller Ruth A, Catchen Julian M, Johnson Eric A, Postlethwait John H

机构信息

Institute of Neuroscience, University of Oregon, Eugene, OR 97403, USA.

出版信息

Dev Biol. 2009 May 1;329(1):1-15. doi: 10.1016/j.ydbio.2009.01.002. Epub 2009 Jan 13.

Abstract

The transcription factor gene Sox9 plays various roles in development, including differentiation of the skeleton, gonads, glia, and heart. Other functions of Sox9 remain enigmatic. Because Sox9 protein regulates expression of target genes, the identification of Sox9 targets should facilitate an understanding of the mechanisms of Sox9 action. To help identify Sox9 targets, we used microarray expression profiling to compare wild-type embryos to mutant embryos lacking activity for both sox9a and sox9b, the zebrafish co-orthologs of Sox9. Candidate genes were further evaluated by whole-mount in situ hybridization in wild-type and sox9 single and double mutant embryos. Results identified genes expressed in cartilage (col2a1a and col11a2), retina (calb2a, calb2b, crx, neurod, rs1, sox4a and vsx1) and pectoral fin bud (klf2b and EST AI722369) as candidate targets for Sox9. Cartilage is a well-characterized Sox9 target, which validates this strategy, whereas retina represents a novel Sox9 function. Analysis of mutant phenotypes confirmed that Sox9 helps regulate the number of Müller glia and photoreceptor cells and helps organize the neural retina. These roles in eye development were previously unrecognized and reinforce the multiple functions that Sox9 plays in vertebrate development.

摘要

转录因子基因Sox9在发育过程中发挥多种作用,包括骨骼、性腺、神经胶质和心脏的分化。Sox9的其他功能仍然未知。由于Sox9蛋白调节靶基因的表达,鉴定Sox9的靶标应有助于理解Sox9的作用机制。为了帮助鉴定Sox9的靶标,我们使用微阵列表达谱分析将野生型胚胎与缺乏sox9a和sox9b活性的突变胚胎进行比较,sox9a和sox9b是Sox9在斑马鱼中的同源基因。通过在野生型、sox9单突变和双突变胚胎中进行全胚胎原位杂交,进一步评估候选基因。结果确定了在软骨(col2a1a和col11a2)、视网膜(calb2a、calb2b、crx、neurod、rs1、sox4a和vsx1)和胸鳍芽(klf2b和EST AI722369)中表达的基因作为Sox9的候选靶标。软骨是一个已被充分表征的Sox9靶标,这验证了该策略,而视网膜代表了Sox9的一种新功能。对突变体表型的分析证实,Sox9有助于调节穆勒神经胶质细胞和光感受器细胞的数量,并有助于组织神经视网膜。这些在眼睛发育中的作用以前未被认识到,进一步证明了Sox9在脊椎动物发育中发挥的多种功能。

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