Chang W, KhosrowShahian F, Chang R, Crawford M J
Department of Biological Sciences, University of Windsor, Ontario, Canada.
Genesis. 2001 Feb;29(2):78-90.
Xenopus Pitx1 is a homeobox gene whose family members are structurally and functionally conserved in organisms as diverse as Drosophila, chick, mouse, human, and frog. Present as a maternal transcript, the gene is zygotically expressed during gastrulation in a dorsal streak of cells. This streak restricts to a small circular domain underlying the center of presumptive neural plate. Shortly thereafter, a crescent of expression develops at the border of anterior neural ectoderm, and as the central plate domain diminishes, the crescent coalesces to define the presumptive cement gland. Expression remains high throughout cement gland development, and subsequently expands to include ectodermal cells involved in stomodeal invagination. During early organogenesis, expression ensues in developing eye, posterior lateral mesoderm, and first branchial arch derivatives. Ectopic expression of xPitx1 causes head deformities including enlarged cement gland, ectopic cement glands, and posterior deformities or, in extreme cases, inhibition of recognizable structures posterior to the cement gland. Expression of markers such as XCG-1, xOtx2, xPax6, neuralbeta tubulin, and xTwist suggest that increases in cement gland and lower mandibular size are likely at the expense of other head tissues. Paradoxically, overexpression is sufficient to partially rescue embryos that are axially perturbed by ultraviolet irradiation or retinoic acid administration. Ectopic expression of xPitx1 in ectodermal explants directly promotes cement gland development as there was no evidence that mesodermal or neural tissue was present in explants.
非洲爪蟾的Pitx1是一种同源异型框基因,其家族成员在果蝇、鸡、小鼠、人类和青蛙等多种生物中在结构和功能上具有保守性。该基因以母源转录本的形式存在,在原肠胚形成期间在一条背侧细胞带中进行合子表达。这条带局限于假定神经板中心下方的一个小圆形区域。此后不久,在前神经外胚层边界处出现一个表达新月形区域,随着中央板区域缩小,新月形区域合并以确定假定的黏附腺。在整个黏附腺发育过程中表达一直很高,随后扩展到包括参与口凹内陷的外胚层细胞。在早期器官发生过程中,在发育中的眼睛、后外侧中胚层和第一鳃弓衍生物中出现表达。xPitx1的异位表达会导致头部畸形,包括黏附腺增大、异位黏附腺以及后部畸形,在极端情况下,会抑制黏附腺后方可识别结构的形成。XCG - 1、xOtx2、xPax6、神经β微管蛋白和xTwist等标记物的表达表明,黏附腺和下颌尺寸的增加可能是以牺牲其他头部组织为代价的。矛盾的是,过表达足以部分挽救因紫外线照射或施用视黄酸而受到轴向干扰的胚胎。在外胚层外植体中xPitx1的异位表达直接促进黏附腺发育,因为没有证据表明外植体中存在中胚层或神经组织。