Alibardi Lorenzo, Toni Mattia
Dipartimento di Biologia evoluzionistica sperimentale, via Selmi 3, University of Bologna, 40126 Bologna, Italy.
Prog Histochem Cytochem. 2008;43(1):1-69. doi: 10.1016/j.proghi.2008.01.001. Epub 2008 Mar 14.
Feathers are the most complex epidermal derivatives among vertebrates. The present review deals with the origin of feathers from archosaurian reptiles, the cellular and molecular aspects of feather morphogenesis, and focus on the synthesis of keratins and associated proteins. Feathers consist of different proteins among which exists a specialized group of small proteins called beta-keratins. Genes encoding these proteins in the chick genome are distributed in different chromosomes, and most genes encode for feather keratins. The latter are here recognized as proteins associated with the keratins of intermediate filaments, and functionally correspond to keratin-associated proteins of hairs, nails and horns in mammals. These small proteins possess unique properties, including resistance and scarce elasticity, and were inherited and modified in feathers from ancestral proteins present in the scales of archosaurian progenitors of birds. The proteins share a common structural motif, the core box, which was present in the proteins of the reptilian ancestors of birds. The core box allows the formation of filaments with a different molecular mechanism of polymerization from that of alpha-keratins. Feathers evolved after the establishment of a special morphogenetic mechanism gave rise to barb ridges. During development, the epidermal layers of feathers fold to produce barb ridges that produce the ramified structure of feathers. Among barb ridge cells, those of barb and barbules initially accumulate small amounts of alpha-keratins that are rapidly replaced by a small protein indicated as "feather keratin". This 10 kDa protein becomes the predominant form of corneous material of feathers. The main characteristics of feather keratins, their gene organization and biosynthesis are similar to those of their reptilian ancestors. Feather keratins allow elongation of feather cells among supportive cells that later degenerate and leave the ramified microstructure of barbs. In downfeathers, barbs are initially independent and form plumulaceous feathers that rest inside a follicle. Stem cells remain in the follicle and are responsible for the regeneration of pennaceous feathers. New barb ridges are produced and they merge to produce a rachis and a flat vane. The modulation of the growth pattern of barb ridges and their fusion into a rachis give rise to a broad variety of feather types, including asymmetric feathers for flight. Feather morphogenesis suggests possible stages for feather evolution and diversification from hair-like outgrowths of the skin found in fossils of pro-avian archosaurians.
羽毛是脊椎动物中最复杂的表皮衍生物。本综述涉及羽毛从祖龙类爬行动物起源、羽毛形态发生的细胞和分子方面,并着重于角蛋白及相关蛋白质的合成。羽毛由不同的蛋白质组成,其中存在一组特殊的小蛋白质,称为β - 角蛋白。在鸡基因组中编码这些蛋白质的基因分布在不同的染色体上,且大多数基因编码羽毛角蛋白。后者在这里被认为是与中间丝角蛋白相关的蛋白质,在功能上对应于哺乳动物毛发、指甲和角中的角蛋白相关蛋白。这些小蛋白质具有独特的特性,包括抗性和稀缺的弹性,并且是从鸟类祖龙类祖先鳞片中存在的祖先蛋白质遗传并在羽毛中修饰而来的。这些蛋白质共享一个共同的结构基序,即核心盒,它存在于鸟类的爬行动物祖先的蛋白质中。核心盒允许形成具有与α - 角蛋白不同聚合分子机制的细丝。在建立了产生羽枝脊的特殊形态发生机制之后,羽毛得以进化。在发育过程中,羽毛的表皮层折叠以产生羽枝脊,从而形成羽毛的分支结构。在羽枝脊细胞中,羽枝和羽小枝的细胞最初积累少量的α - 角蛋白,这些α - 角蛋白很快被一种被称为“羽毛角蛋白”的小蛋白质所取代。这种10 kDa的蛋白质成为羽毛角质材料的主要形式。羽毛角蛋白的主要特征、它们的基因组织和生物合成与它们的爬行动物祖先相似。羽毛角蛋白允许羽毛细胞在支持细胞中伸长,这些支持细胞随后退化并留下羽枝的分支微观结构。在绒羽中,羽枝最初是独立的,形成绒羽状羽毛,位于毛囊内。干细胞保留在毛囊中,并负责正羽的再生。新的羽枝脊产生并合并形成羽轴和平展的羽片。羽枝脊生长模式的调节及其融合成羽轴导致了各种各样的羽毛类型,包括用于飞行的不对称羽毛。羽毛形态发生暗示了羽毛从原始鸟类祖龙化石中发现的皮肤毛发状突出物进化和多样化的可能阶段。