首页> 美国卫生研究院文献>Proceedings of the National Academy of Sciences of the United States of America >Ol-Prx 3 a member of an additional class of homeobox genes is unimodally expressed in several domains of the developing and adult central nervous system of the medaka (Oryzias latipes)
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Ol-Prx 3 a member of an additional class of homeobox genes is unimodally expressed in several domains of the developing and adult central nervous system of the medaka (Oryzias latipes)

机译:Ol-Prx 3是另一类同源异型盒基因的成员在青aka(Oryzias latipes)的发育中和成年中枢神经系统的多个域中单峰表达

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摘要

Large-scale genetic screens for mutations affecting early neurogenesis of vertebrates have recently been performed with an aquarium fish, the zebrafish. Later stages of neural morphogenesis have attracted less attention in small fish species, partly because of the lack of molecular markers of developing structures that may facilitate the detection of discrete structural alterations. In this context, we report the characterization of Ol-Prx 3 (Oryzias latipes-Prx 3). This gene was isolated in the course of a large-scale screen for brain cDNAs containing a highly conserved DNA binding region, the homeobox helix-three. Sequence analysis revealed that this gene belongs to another class of homeobox genes, together with a previously isolated mouse ortholog, called OG-12 [Rovescalli, A. C., Asoh, S. & Nirenberg, M. (1996) Proc. Natl. Acad. Sci. USA 93, 10691–10696] and with the human SHOX gene [Rao, E., Weiss, B., Fukami, M., Rump, A., Niesler, B., et al. (1997) Nat. Genet. 16, 54–62], thought to be involved in the short-stature phenotype of Turner syndrome patients. These three genes exhibit a moderate level of identity in the homeobox with the other genes of the paired-related (PRX) gene family. Ol-Prx 3, as well as the PRX genes, are expressed in various cartilaginous structures of head and limbs. These genes might thus be involved in common regulatory pathways during the morphogenesis of these structures. Moreover, this paper reports a complex and monophasic pattern of Ol-Prx 3 expression in the central nervous system, which differs markedly from the patterns reported for the PRX genes, Prx 3 excluded: this gene begins to be expressed in a variety of central nervous system territories at late neurula stage. Strikingly, it remains turned on in some of the derivatives of each territory during the entire life of the fish. We hope this work will thus help identify common features for the PRX 3 family of homeobox genes.
机译:最近使用水族馆鱼斑马鱼对影响脊椎动物早期神经发生的突变进行了大规模遗传筛选。神经形态发生的后期阶段在小型鱼类中引起了较少的关注,部分原因是缺乏发育中的结构的分子标记,这些分子标记可能有助于检测离散的结构改变。在这种情况下,我们报告Ol-Prx 3(Oryzias latipes-Prx 3)的表征。该基因是在大规模筛选含有高度保守的DNA结合区即同源盒三螺旋的脑cDNA的过程中分离出来的。序列分析表明,该基因与先前分离的小鼠直系同源基因,称为OG-12,属于同种异型框基因的另一类[Rovescalli,A.C.,Asoh,S。&Nirenberg,M。(1996)Proc.Natl.Acad.Sci.USA 90:5873-5877。 Natl。学院科学USA 93,10691–10696]和人类SHOX基因[Rao,E.,Weiss,B.,Fukami,M.,Rump,A.,Niesler,B.等。 (1997)Nat。基因[16,54–62],被认为与特纳综合征患者的矮身表型有关。这三个基因在同源异型盒中与配对相关(PRX)基因家族的其他基因具有中等程度的同一性。 Ol-Prx 3以及PRX基因在头和四肢的各种软骨结构中表达。因此,这些基因可能在这些结构的形态发生过程中参与共同的调控途径。此外,本文报道了中枢神经系统中Ol-Prx 3表达的复杂和单相模式,与报告的PRX基因的模式显着不同,Prx 3被排除在外:该基因开始在多种中枢神经中表达在神经末期的系统领土。引人注目的是,在鱼类的整个生命周期中,每个区域的某些衍生物中都将其保持打开状态。我们希望这项工作将有助于鉴定PRX 3同源盒基因家族的共同特征。

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