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转录因子鸡Scratch2在一部分有丝分裂后早期神经祖细胞中表达。

The transcription factor chicken Scratch2 is expressed in a subset of early postmitotic neural progenitors.

作者信息

Vieceli Felipe Monteleone, Simões-Costa Marcos, Turri José Antonio, Kanno Tatiane, Bronner Marianne, Yan Chao Yun Irene

机构信息

Department of Cell and Developmental Biology, Universidade de São Paulo, São Paulo, SP, Brazil.

出版信息

Gene Expr Patterns. 2013 Jun-Jul;13(5-6):189-96. doi: 10.1016/j.gep.2013.03.004. Epub 2013 Apr 6.

Abstract

Scratch proteins are members of the Snail superfamily which have been shown to regulate invertebrate neural development. However, in vertebrates, little is known about the function of Scratch or its relationship to other neural transcription factors. We report the cloning of chicken Scratch2 (cScrt2) and describe its expression pattern in the chick embryo from HH15 through HH29. cScrt2 was detected in cranial ganglia, the nasal placode and neural tube. At all stages examined, cScrt2 expression is only detected within a subregion of the intermediate zone of the neural tube. cScrt2 is also expressed in the developing dorsal root ganglia from HH22-23 onwards and becomes limited to its dorsal medial domain at HH29. phospho-Histone H3 and BrdU-labeling revealed that the cScrt2 expression domain is located immediately external to the proliferative region. In contrast, cScrt2 domain overlapped almost completely with that of the postmitotic neural transcription factor NeuroM/Ath3/NEUROD4. Together, these data define cScrt2-positive cells as a subset of immediately postmitotic neural progenitors. Previous data has shown that Scrt2 is a repressor of E-box-driven transcription whereas NeuroM is an E-box-transactivator. In light of these data, the co-localization detected here suggests that Scrt2 and NeuroM may have opposing roles during definition of neural subtypes.

摘要

Scratch蛋白是Snail超家族的成员,已被证明可调节无脊椎动物的神经发育。然而,在脊椎动物中,关于Scratch的功能及其与其他神经转录因子的关系知之甚少。我们报告了鸡Scratch2(cScrt2)的克隆,并描述了其在HH15至HH29期鸡胚中的表达模式。在颅神经节、鼻基板和神经管中检测到cScrt2。在所有检测阶段,仅在神经管中间带的一个子区域内检测到cScrt2表达。cScrt2在HH22 - 23期开始的发育中的背根神经节中也有表达,并在HH29期局限于其背内侧区域。磷酸化组蛋白H3和BrdU标记显示,cScrt2表达域位于增殖区域的紧邻外侧。相比之下,cScrt2域几乎与有丝分裂后神经转录因子NeuroM/Ath3/NEUROD4的域完全重叠。这些数据共同将cScrt2阳性细胞定义为紧邻有丝分裂后神经祖细胞的一个子集。先前的数据表明,Scrt2是E盒驱动转录的抑制因子,而NeuroM是E盒反式激活因子。鉴于这些数据,此处检测到的共定位表明Scrt2和NeuroM在神经亚型的定义过程中可能具有相反的作用。

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