蝴蝶拟态超基因的功能遗传要素。

IF 9.1 1区 综合性期刊 Q1 MULTIDISCIPLINARY SCIENCES
Nicholas W VanKuren,Sofia I Sheikh,Claire L Fu,Darli Massardo,Namiko N Service,Wei Lu,Marcus R Kronforst
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引用次数: 0

摘要

发育需要跨越空间和时间的许多基因的协调作用,然而许多物种可以发展离散的,交替的表型。这种复杂的平衡多态性通常由超基因控制:多个紧密相连的基因座共同控制复杂表型的发育。超基因在自然界广泛存在。然而,超基因等位基因的进化和功能仍然不清楚,因为功能位点的身份和它们之间的致病变异仍然是未知的。双性表基因控制凤蝶和凤蝶的拟态多态性。交替的等位基因导致离散的模拟或非模拟翅膀模式的发展。我们发现,模仿等位基因通过获得6个新的顺式调控元件(cre)和一个反转将这些cre与dsx和新的非编码基因U3X锁定在一起而进化。这些新的cre中至少有四种是dsx表达和模仿模式发展所必需的。DSX结合的全基因组分析表明,DSX通过直接调节自身和少数非连锁基因的表达来控制模拟模式的发育。因此,dsx超基因包含多个功能遗传元件,每个元件都是表型转换所必需的,并且通过反转连接在一起,并且可能通过直接调节未连接的“修饰”基因来影响颜色图案的发育。因此,我们的研究结果支持了经典的超基因进化理论,但更新了这些理论,使其与半个多世纪前我们对基因调控的了解相匹配。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Functional genetic elements of a butterfly mimicry supergene.
Development requires the coordinated action of many genes across space and time, yet numerous species can develop discrete, alternate phenotypes. Such complex balanced polymorphisms are often controlled by supergenes: multiple tightly linked loci that function together to control development of a complex phenotype. Supergenes are widespread in nature. However, the evolution and functions of supergene alleles remain obscure because the identities of the functional loci, and the causative variation between them, remain essentially unknown. The doublesex supergene controls mimicry polymorphism in the swallowtail butterflies Papilio polytes and Papilio alphenor. Alternate alleles cause development of discrete mimetic or nonmimetic wing patterns. We found that the mimetic allele evolved by gaining six new cis-regulatory elements (CREs) and an inversion that locked those CREs together with dsx and the novel noncoding gene U3X. At least four of these new CREs are essential for dsx expression and mimetic pattern development. Genome-wide assays of DSX binding suggest that dsx controls mimetic pattern development by directly regulating the expression of both itself and a handful of unlinked genes. The dsx supergene thus contains multiple functional genetic elements, each required for the phenotype switch and linked together by an inversion, and likely exerts its effects on color pattern development through direct regulation of unlinked "modifier" genes. Our results therefore support classic theories of supergene evolution, but update those ideas to match what we have learned about gene regulation since their development over a half century ago.
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来源期刊
CiteScore
19.00
自引率
0.90%
发文量
3575
审稿时长
2.5 months
期刊介绍: The Proceedings of the National Academy of Sciences (PNAS), a peer-reviewed journal of the National Academy of Sciences (NAS), serves as an authoritative source for high-impact, original research across the biological, physical, and social sciences. With a global scope, the journal welcomes submissions from researchers worldwide, making it an inclusive platform for advancing scientific knowledge.
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