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Hox 基因簇 3 旁系同源基因调控胸腺、甲状腺和甲状旁腺的发育与迁移。

Hox group 3 paralogs regulate the development and migration of the thymus, thyroid, and parathyroid glands.

作者信息

Manley N R, Capecchi M R

机构信息

Howard Hughes Medical Institute, Department of Human Genetics, University of Utah School of Medicine, Salt Lake City 84112-5331.

出版信息

Dev Biol. 1998 Mar 1;195(1):1-15. doi: 10.1006/dbio.1997.8827.

Abstract

The thymus, thyroid, and parathyroid glands in vertebrates develop from the pharyngeal region, with contributions both from pharyngeal endoderm and from neural crest cells in the pharyngeal arches. Hoxa3 mutant homozygotes have defects in the development of all three organs. Roles for the Hoxa3 paralogs, Hoxb3 and Hoxd3, were investigated by examining various mutant combinations. The thyroid defects seen in Hoxa3 single mutants are exacerbated in double mutants with either of its paralogs, although none of the double-mutant combinations resulted in thyroid agenesis. The results indicate that the primary role of these genes in thyroid development is their effect on the development and migration of the ultimobranchial bodies, which contribute the parafollicular or C-cells to the thyroid. Hoxb3, Hoxd3 double mutants show no obvious defects in the thymus or parathyroids. However, the removal of one functional copy of Hoxa3 from the Hoxb3, Hoxd3 double mutants (Hoxa3 +/-, Hoxb3-/-, Hoxd3-/-) results in the failure of the thymus and parathyroid glands to migrate to their normal positions in the throat. Very little is known about the molecular mechanisms used to mediate the movement of tissues during development. These results indicate that Hoxa3, Hoxb3, and Hoxd3 have highly overlapping functions in mediating the migration of pharyngeal organ primordia. In addition, Hoxa3 has a unique function with respect to its paralogs in thymus, parathyroid, and thyroid development. This unique function may be conferred by the expression of Hoxa3, but not Hoxb3 nor Hoxd3, in the pharyngeal pouch endoderm.

摘要

脊椎动物的胸腺、甲状腺和甲状旁腺由咽区发育而来,咽内胚层和咽弓中的神经嵴细胞都参与其中。Hoxa3突变纯合子在这三个器官的发育中都存在缺陷。通过研究各种突变组合,对Hoxa3的旁系同源基因Hoxb3和Hoxd3的作用进行了研究。在Hoxa3单突变体中出现的甲状腺缺陷,在与任一其旁系同源基因的双突变体中会加剧,尽管没有一种双突变组合导致甲状腺发育不全。结果表明,这些基因在甲状腺发育中的主要作用是它们对终末鳃体发育和迁移的影响,终末鳃体为甲状腺贡献滤泡旁细胞或C细胞。Hoxb3、Hoxd3双突变体在胸腺或甲状旁腺中未表现出明显缺陷。然而,从Hoxb3、Hoxd3双突变体(Hoxa3 +/-, Hoxb3-/-, Hoxd3-/-)中去除一个Hoxa3功能拷贝会导致胸腺和甲状旁腺无法迁移到喉咙中的正常位置。关于发育过程中用于介导组织运动的分子机制,人们知之甚少。这些结果表明,Hoxa3、Hoxb3和Hoxd3在介导咽器官原基的迁移中具有高度重叠的功能。此外,Hoxa3在胸腺、甲状旁腺和甲状腺发育方面相对于其旁系同源基因具有独特功能。这种独特功能可能由Hoxa3在咽囊内胚层中的表达赋予,而Hoxb3和Hoxd3则没有。

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