Collaborative research: Understanding the role of developmental bias in the morphological diversification of bat molars
Collaborative research: Understanding the role of developmental bias in the morphological diversification of bat molars
批准号:
2017803
负责人:
Karen Sears
金额:
$59.66万
依托单位国家:
美国
项目类别:
Standard Grant
财政年份:
2020
资助国家:
美国
项目状态:
已结题
起止时间:
2020-08-01 至 2023-07-31
中文摘要
点击翻译按钮获取中文摘要
英文摘要
The evolution of animal form has been uneven, radiating in fits and starts, and exploring some forms but not others. Why this pattern exists has long been a fundamental question in biology. One possible explanation can be found in the very nature of the way that animals grow from an egg into an adult, i.e., in their development. The genes that control animal development interact in networks. Some genes in these networks interact with many other genes, while others are more peripheral and isolated. This project tests the hypothesis that most evolution in animal form occurs through changes in peripheral network components, and in the aspects of form that those peripheral components make, while central genes and their associated forms are conserved among species. To test this hypothesis, this project investigates the patterns and drivers of tooth evolution in an ecologically diverse animal group, noctilionoid bats. This project is expected to be among the first to characterize the organization of the gene networks that control animal form, and the impact that this organization has on the way evolution proceeds. This project is therefore expected to illuminate mechanisms that have shaped the evolution of animals over the history of life on earth. This project will also directly increase participation of students from underrepresented groups (URMs) in research and contribute to public education. These goals will be achieved by involving URM undergraduates from Puerto Rico in project research, training postdoctoral scientists in URM mentorship, and showcasing project results at the Burke Museum.This project’s goal is to characterize and model the evolution of developmental GRN modules and resulting morphologies, using the radiation of noctilionoid bats and their molars as a model system. This project's central hypothesis is that a conserved core module of the molar GRN controls the initial formation of molar traits that are conserved across species, with evolutionary modification of network sub-modules leading to interspecific morphological variation. To test this, two aims will be completed. In Aim 1, the team will quantify morphology of developing lower first molars (m1) in representative noctilionoids, and adult m1s across all extant noctilionoid genera. Data will be used to reconstruct the development and evolution of noctilionoid m1 morphology, and identify conserved and variable traits over developmental and evolutionary time. In Aim 2, the team will map gene expression over m1 development in representative noctilionoids, functionally test the ability of observed expression differences in key molar developmental pathways to generate variable m1 morphologies, reconstruct GRN modules for bat m1s in computational space, and link GRN modules to m1 morphological diversity. Using data from both aims, the team will also use machine-learning techniques to reverse-engineer a computational model that will predict m1 phenotypes resulting from variation in developmental modules. Through this research, this project will characterize the role of developmental biases in morphological evolution within an adaptive radiation, functionally link shifts in gene expression to the evolution of morphology among closely related species, and generate a predictive model for morphological evolution across a hyper-diverse mammal groupThis 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.
期刊论文(7)
专著(0)
科研奖励(0)
会议论文
DOI:
10.1038/s43587-023-00462-6
发表时间:
2023-09
期刊:
INNOVATION IN AGING
影响因子:
7
作者:
[Lu, Viviana Perez Ake, Fei, Zhe, Raj, Ken, Horvath, Steve]
通讯作者:
Horvath, Steve
Bat Dentitions: A Model System for Studies at the Interface of Development, Biomechanics, and Evolution
蝙蝠牙列:发育、生物力学和进化界面研究的模型系统
DOI:
10.1093/icb/icac042
发表时间:
2022
期刊:
Integrative And Comparative Biology
影响因子:
2.6
作者:
[Santana, Sharlene E., Grossnickle, David M., Sadier, Alexa, Patterson, Edward, Sears, Karen E.]
通讯作者:
Sears, Karen E.
Grand Challenges in Comparative Tooth Biology
比较牙齿生物学的巨大挑战
DOI:
10.1093/icb/icaa038
发表时间:
2020
期刊:
Integrative and Comparative Biology
影响因子:
2.6
作者:
[Hulsey, C Darrin, Cohen, Karly E, Johanson, Zerina, Karagic, Nidal, Meyer, Axel, Miller, Craig T, Sadier, Alexa, Summers, Adam P, Fraser, Gareth J]
通讯作者:
Fraser, Gareth J
Dimensions: Collaborative Research: Discovering genomic and developmental mechanisms that underlie sensory innovations critical to adaptive diversification
-
批准号:1854469
-
项目类别:Continuing Grant
-
资助金额:$23.09万
-
财政年份:2017
-
负责人:Karen Sears
-
依托单位:
DISSERTATION RESEARCH: Mechanisms of Mammalian Middle Ear Ossicle Transition from the Reptilian Jaw Joint
-
批准号:1406802
-
项目类别:Standard Grant
-
资助金额:$1.99万
-
财政年份:2014
-
负责人:Karen Sears
-
依托单位:
Dimensions: Collaborative Research: Discovering genomic and developmental mechanisms that underlie sensory innovations critical to adaptive diversification
-
批准号:1442314
-
项目类别:Continuing Grant
-
资助金额:$79.85万
-
财政年份:2014
-
负责人:Karen Sears
-
依托单位:
Collaborative Research: Genetic Determinants of MammalianLlimb Biodiversity
-
批准号:1257873
-
项目类别:Continuing Grant
-
资助金额:$52.0万
-
财政年份:2013
-
负责人:Karen Sears
-
依托单位:
国内基金
海外基金
登录
查看更多内容
Research on Quantum Field Theory without a Lagrangian Description
-
批准号:24ZR1403900
-
项目类别:省市级项目
-
资助金额:--
-
批准年份:2024
-
负责人:SATOSHI NAWATA
-
依托单位:
HIF-1α调控软骨细胞衰老在骨关节炎进展中的作用及机制研究
-
批准号:82371603
-
项目类别:面上项目
-
资助金额:49.00万元
-
批准年份:2023
-
负责人:陈晓
-
依托单位:
PRNP调控巨噬细胞M2极化并减弱吞噬功能促进子宫内膜异位症进展的机制研究
-
批准号:82371651
-
项目类别:面上项目
-
资助金额:49.00万元
-
批准年份:2023
-
负责人:赵栋
-
依托单位:
脐带间充质干细胞微囊联合低能量冲击波治疗神经损伤性ED的机制研究
-
批准号:82371631
-
项目类别:面上项目
-
资助金额:49.00万元
-
批准年份:2023
-
负责人:卢慕峻
-
依托单位:
TIPE2调控巨噬细胞M2极化改善睑板腺功能障碍的作用机制研究
-
批准号:82371028
-
项目类别:面上项目
-
资助金额:49.00万元
-
批准年份:2023
-
负责人:赵慧
-
依托单位:
超声驱动压电效应激活门控离子通道促眼眶膜内成骨的作用及机制研究
-
批准号:82371103
-
项目类别:面上项目
-
资助金额:49.00万元
-
批准年份:2023
-
负责人:阮静
-
依托单位:
Lienard系统的不变代数曲线、可积性与极限环问题研究
-
批准号:12301200
-
项目类别:青年科学基金项目
-
资助金额:30.00万元
-
批准年份:2023
-
负责人:钱欣洁
-
依托单位:
骨髓ISG+NAMPT+中性粒细胞介导抗磷脂综合征B细胞异常活化的机制研究
-
批准号:82371799
-
项目类别:面上项目
-
资助金额:47.00万元
-
批准年份:2023
-
负责人:杨程德
-
依托单位:
利用CRISPR内源性激活Atoh1转录促进前庭毛细胞再生和功能重建
-
批准号:82371145
-
项目类别:面上项目
-
资助金额:46.00万元
-
批准年份:2023
-
负责人:陶永
-
依托单位:
Idh3a作为线粒体代谢—表观遗传检查点调控产热脂肪功能的机制研究
-
批准号:82370851
-
项目类别:面上项目
-
资助金额:48.00万元
-
批准年份:2023
-
负责人:包玉倩
-
依托单位: