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B1 SOX 通过在早期斑马鱼胚胎中的模式形成和形态发生来协调细胞特化。

B1 SOX coordinate cell specification with patterning and morphogenesis in the early zebrafish embryo.

机构信息

Graduate School of Frontier Biosciences, Osaka University, Suita, Japan.

出版信息

PLoS Genet. 2010 May 6;6(5):e1000936. doi: 10.1371/journal.pgen.1000936.

Abstract

The B1 SOX transcription factors SOX1/2/3/19 have been implicated in various processes of early embryogenesis. However, their regulatory functions in stages from the blastula to early neurula remain largely unknown, primarily because loss-of-function studies have not been informative to date. In our present study, we systematically knocked down the B1 sox genes in zebrafish. Only the quadruple knockdown of the four B1 sox genes sox2/3/19a/19b resulted in very severe developmental abnormalities, confirming that the B1 sox genes are functionally redundant. We characterized the sox2/3/19a/19b quadruple knockdown embryos in detail by examining the changes in gene expression through in situ hybridization, RT-PCR, and microarray analyses. Importantly, these phenotypic analyses revealed that the B1 SOX proteins regulate the following distinct processes: (1) early dorsoventral patterning by controlling bmp2b/7; (2) gastrulation movements via the regulation of pcdh18a/18b and wnt11, a non-canonical Wnt ligand gene; (3) neural differentiation by regulating the Hes-class bHLH gene her3 and the proneural-class bHLH genes neurog1 (positively) and ascl1a (negatively), and regional transcription factor genes, e.g., hesx1, zic1, and rx3; and (4) neural patterning by regulating signaling pathway genes, cyp26a1 in RA signaling, oep in Nodal signaling, shh, and mdkb. Chromatin immunoprecipitation analysis of the her3, hesx1, neurog1, pcdh18a, and cyp26a1 genes further suggests a direct regulation of these genes by B1 SOX. We also found an interesting overlap between the early phenotypes of the B1 sox quadruple knockdown embryos and the maternal-zygotic spg embryos that are devoid of pou5f1 activity. These findings indicate that the B1 SOX proteins control a wide range of developmental regulators in the early embryo through partnering in part with Pou5f1 and possibly with other factors, and suggest that the B1 sox functions are central to coordinating cell fate specification with patterning and morphogenetic processes occurring in the early embryo.

摘要

B1 SOX 转录因子 SOX1/2/3/19 被认为参与了早期胚胎发生的各种过程。然而,它们在囊胚到早期神经胚阶段的调控功能在很大程度上仍然未知,主要是因为迄今为止的功能丧失研究并没有提供信息。在我们目前的研究中,我们系统地在斑马鱼中敲低了 B1 sox 基因。只有 B1 sox 基因 sox2/3/19a/19b 的四重敲低导致了非常严重的发育异常,这证实了 B1 sox 基因在功能上是冗余的。我们通过原位杂交、RT-PCR 和微阵列分析来检查基因表达的变化,详细地描述了 sox2/3/19a/19b 四重敲低胚胎的特征。重要的是,这些表型分析表明,B1 SOX 蛋白调节以下不同的过程:(1)通过控制 bmp2b/7 来调节早期背腹模式;(2)通过调节 pcdh18a/18b 和 wnt11(一种非经典的 Wnt 配体基因)来调节原肠胚运动;(3)通过调节 Hes 类 bHLH 基因 her3 和神经前类 bHLH 基因 neurog1(正调控)和 ascl1a(负调控)以及区域转录因子基因,如 hesx1、zic1 和 rx3,来调节神经分化;(4)通过调节信号通路基因,如 RA 信号通路中的 cyp26a1、Nodal 信号通路中的 oep、shh 和 mdkb,来调节神经模式。her3、hesx1、neurog1、pcdh18a 和 cyp26a1 基因的染色质免疫沉淀分析进一步表明,这些基因直接受到 B1 SOX 的调控。我们还发现,B1 sox 四重敲低胚胎的早期表型与缺乏 pou5f1 活性的母体-合子 spg 胚胎之间存在有趣的重叠。这些发现表明,B1 SOX 蛋白通过与 Pou5f1 部分合作,并可能与其他因素合作,在早期胚胎中控制广泛的发育调节剂,这表明 B1 sox 功能对于协调细胞命运特化与早期胚胎中发生的模式形成和形态发生过程至关重要。

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