Carroll T J, Vize P D
Cell and Developmental Biology, University of Texas, Austin, Texas, 78712, USA.
Dev Biol. 1999 Oct 1;214(1):46-59. doi: 10.1006/dbio.1999.9414.
Pax genes encode a family of highly conserved DNA-binding transcription factors. These proteins play key roles in regulating a number of vertebrate and invertebrate developmental processes. Mutations in Pax-6 result in eye defects in flies, mice, and humans, and ectopic expression of this gene can trigger the development of ectopic compound eyes in flies. Likewise, mutation of other Pax genes in vertebrates results in the failure of specific differentiation programs-Pax-1 causes skeletal defects; Pax-2, kidney defects; Pax-3 or Pax-7, neural crest defects; Pax-4, pancreatic beta-cell defects; Pax-5, B-cell defects; Pax-8, thyroid defects; and Pax-9, tooth defects. Although this class of genes is obviously required for the normal differentiation of a number of distinct organ systems, they have not previously been demonstrated to be capable of directing the embryonic development of organs in vertebrates. In this report, it is demonstrated that Pax-8 plays such a role in the establishment of the Xenopus embryonic kidney, the pronephros. However, in order to efficiently direct cells to form pronephric kidneys, XPax-8 requires cofactors, one of which may be the homeobox transcription factor Xlim-1. These two genes are initially expressed in overlapping domains in late gastrulae, and cells expressing both genes will go on to form the kidney. Ectopic expression of either gene alone has a moderate effect on pronephric patterning, while coexpression of XPax-8 plus Xlim-1 results in the development of embryonic kidneys of up to five times normal complexity and also leads to the development of ectopic pronephric tubules. This effect was synergistic rather than additive. XPax-2 can also synergize with Xlim-1, but the expression profile of this gene indicates that it normally functions later in pronephric development than does XPax-8. Together these data indicate that the interaction between XPax-8 and Xlim-1 is a key early step in the establishment of the pronephric primordium.
Pax基因编码一类高度保守的DNA结合转录因子。这些蛋白质在调节许多脊椎动物和无脊椎动物的发育过程中发挥关键作用。Pax - 6基因的突变会导致果蝇、小鼠和人类出现眼部缺陷,而该基因的异位表达会在果蝇中引发异位复眼的发育。同样,脊椎动物中其他Pax基因的突变会导致特定分化程序的失败——Pax - 1导致骨骼缺陷;Pax - 2导致肾脏缺陷;Pax - 3或Pax - 7导致神经嵴缺陷;Pax - 4导致胰腺β细胞缺陷;Pax - 5导致B细胞缺陷;Pax - 8导致甲状腺缺陷;Pax - 9导致牙齿缺陷。尽管这类基因显然是许多不同器官系统正常分化所必需的,但此前尚未证明它们能够指导脊椎动物器官的胚胎发育。在本报告中,证明了Pax - 8在非洲爪蟾胚胎肾脏(前肾)的形成中发挥这样的作用。然而,为了有效地引导细胞形成前肾,XPax - 8需要辅助因子,其中之一可能是同源框转录因子Xlim - 1。这两个基因最初在晚期原肠胚中以重叠区域表达,同时表达这两个基因的细胞将继续形成肾脏。单独异位表达任何一个基因对前肾模式形成有中等影响,而XPax - 8与Xlim - 1共表达会导致胚胎肾脏发育到正常复杂程度的五倍,还会导致异位前肾小管的发育。这种效应是协同的而非累加的。XPax - 2也能与Xlim - 1协同作用,但该基因的表达谱表明它在前肾发育中通常比XPax - 8发挥作用的时间更晚。这些数据共同表明,XPax - 8与Xlim - 1之间的相互作用是前肾原基形成早期的关键步骤。