Developmental Mechanisms of Scale Loss and Replacement in the Evolution of Catfishes
Developmental Mechanisms of Scale Loss and Replacement in the Evolution of Catfishes
批准号:
1755305
负责人:
David Stock
金额:
$58.8万
依托单位国家:
美国
项目类别:
Standard Grant
财政年份:
2018
资助国家:
美国
项目状态:
已结题
起止时间:
2018-09-15 至 2024-08-31
中文摘要
一般认为,在进化过程中,结构的丢失伴随着产生它所需的遗传信息的丢失,从而阻止了它的再现。对于这种不可逆转的进化,一个明显的例外是鲶鱼表皮的进化。这一群体的共同祖先失去了鳞片的外骨骼,导致大多数现存物种的“裸露”皮肤特征。然而,在几种“装甲”鲶鱼的皮肤中,一种外部骨骼以被称为鳞甲的骨板的形式重新出现。这个项目测试的假设,使鳞片的遗传程序保留在一个潜在的形式在裸鲶鱼和重新激活的装甲鲶鱼盾的起源。确定生物体对过去适应的遗传“记忆”的程度,将有助于了解物种对环境变化作出进化而不是灭绝反应的能力。该项目将为本科生、研究生和博士后学员提供研究机会,并为加强首席研究员在遗传学和鱼类生物学方面的本科课程提供材料。这项工作将利用维持的鱼群向中小学生介绍鲶鱼的各种不寻常的生殖行为。最后,将在科罗拉多大学自然历史博物馆举办一次关于鱼鳞结构和演变的展览(包括博物馆创始人一百多年前进行的相关工作)。保留和重新激活的遗传程序的鲶鱼的躯干真皮骨骼的程度和性质进行了研究,通过比较基因的表达和调节在斑马鱼(代表祖先的规模条件),两种裸鲶鱼和两种装甲鲶鱼。通过原位杂交分析验证了裸鲶鱼鳞片起始基因表达缺失,而甲鲶鳞片起始基因表达恢复的假设。调节祖先鳞片中基因表达的顺式调节元件和/或反式作用因子已在裸鲶鱼中保留并被用于盾的发育,这一假设将通过对多个物种幼虫中的斑马鱼和鲶鱼基因侧翼DNA的报告转基因分析来检验。这些报告基因转基因实验,结合使用基于CRISPR/Cas9的基因组编辑删除斑马鱼顺式调控元件,还将提供对元件多效性功能的深入了解,这是一种可能在缺乏性状表达的情况下保留它们的特征。使用保守的遗传程序的复杂结构的经常性起源,作为假设的系统正在研究中,已被标记为“深度同源性”,它的发现代表了进化发育生物学的胜利之一。这项研究将有助于理解深层同源性,不仅在基因表达的普遍研究水平上,而且在潜在的基因组元素上也是如此。该奖项反映了NSF的法定使命,并通过使用基金会的智力价值和更广泛的影响审查标准进行评估,被认为值得支持。
英文摘要
It is generally thought that the loss of a structure in evolution is accompanied by the loss of the genetic information needed to produce it, thereby preventing its reappearance. An apparent exception to such irreversibility of evolution is provided by the evolution of the skin covering of catfishes. A common ancestor of this group lost its outer skeleton of scales, resulting in the "naked" skin characteristic of most living species. An outer skeleton has reappeared in the skin of several families of "armored" catfishes, however, in the form of bony plates known as scutes. This project tests the hypothesis that the genetic program for making scales is retained in a latent form in naked catfishes and was reactivated in the origin of armored catfish scutes. Determining the extent to which organisms possess a genetic "memory" of past adaptations will provide insight into the ability of species to respond to environmental change with evolution rather than extinction. The project will provide research opportunities for undergraduate, graduate, and post-doctoral trainees, as well as materials for enhancing the principal investigator's undergraduate courses in genetics and fish biology. Fish colonies maintained for the work will be used to introduce primary and secondary school students to a variety of unusual reproductive behaviors employed by catfishes. Finally, an exhibit will be prepared at the University of Colorado Natural History Museum on the structure and evolution of fish scales (including relevant work by the museum's founder conducted over a hundred years ago). The degree and nature of retention and reactivation of genetic programs for the trunk dermal skeleton in catfishes will be investigated by comparison of gene expression and regulation in the zebrafish (representing the ancestral scaled condition), two species of naked catfishes and two species of armored catfishes. The hypothesis that the expression of scale initiation genes was lost in naked catfishes and regained in the scutes of armored catfishes will be tested by in situ hybridization analysis. The hypothesis that cis-regulatory elements and/or trans-acting factors regulating gene expression in ancestral scales have been retained in naked catfishes and co-opted for the development of scutes will be tested by reporter transgenic analysis of DNA flanking zebrafish and catfish genes in larvae of multiple species. These reporter transgenic experiments, combined with deletion of zebrafish cis-regulatory elements using CRISPR/Cas9-based genome editing, will also provide insight into pleiotropic function of the elements, a feature likely to preserve them in the absence of trait expression. Recurrent origin of complex structures using conserved genetic programs, as hypothesized for the system under study, has been labeled "deep homology" and its discovery represents one of the triumphs of Evolutionary Developmental Biology. The proposed research will contribute to the understanding of deep homology not only at the commonly studied level of gene expression but at that of the underlying genomic elements as well.This award reflects NSF's statutory mission and has been deemed worthy of support through evaluation using the Foundation's intellectual merit and broader impacts review criteria.
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