Collaborative research: Origin of multicellular complexity in experimentally-evolved Saccharomyces cerevisiae
Collaborative research: Origin of multicellular complexity in experimentally-evolved Saccharomyces cerevisiae
批准号:
1656549
负责人:
William Ratcliff
金额:
$63.88万
依托单位国家:
美国
项目类别:
Continuing Grant
财政年份:
2017
资助国家:
美国
项目状态:
已结题
起止时间:
2017-02-01 至 2021-01-31
中文摘要
复杂的多细胞生命是如何从定义了地球上数十亿年生命的单细胞微生物中产生的?多细胞生物的兴起推动了生命的深刻多样化,从根本上改变了地球的生态,但人们对这一重大进化转变是如何发生的知之甚少。这在很大程度上是因为大多数多细胞谱系都是古老的,这种转变的早期步骤已经被灭绝所掩盖。PI已经克服了这一限制,开发了一种新的实验室系统,通过实验在面包酵母中进化出简单的多细胞。经过数千代的实验室进化,这些形成集群的“雪花酵母”进化出一套多细胞适应性,包括更大的集群大小、更高的细胞程序性死亡速度和更具流体动力学的特征。PI将使用这个模型系统来检验新的多细胞特征是如何在进化中产生的,并将确定基本的发育机制,即大多数多细胞生物所经历的单细胞瓶颈(例如,单个受精卵),是否提高了自然选择作用于这些新出现的多细胞特征的能力。这项跨学科的工作利用了实验进化、下一代测序、分子遗传学、共聚焦显微镜、图像分析和数学建模方面的尖端技术。通过阐明向多细胞进化过渡的最早步骤,拟议的研究将有助于解决对生物学至关重要的一个突出问题。生物学复杂性的进化仍然很难教授,特别是在高中阶段。该奖项将支持开发一种适用于高中和大学课堂的新型实验模块,在该模块中,学生使用雪花酵母和计算机模拟来研究多细胞的进化。PI将在夏季举办校园研讨会,培训亚特兰大地区的教师使用这门课程。最近的实验表明,单细胞生物体很容易进化成多细胞集群,但人们对细胞集群如何随后演变为更大的多细胞复杂性知之甚少。这项拟议的研究通过提出以下问题直接解决了这个问题:当突变和重组只能直接影响细胞水平的表型时,多细胞特征是如何在进化中出现的?早期发育机制能否进化以促进对这些新出现的多细胞特征的选择?如何为发育功能招募基因,以及如何将新的多细胞适应整合到整个生物体的形式和功能中?回答上述问题将提供对多细胞复杂性进化起源的根本洞察,并将为其他重大进化转变的类似研究提供理论基础。雪花酵母是这项工作的理想实验系统:PI已经进化出大量的形态新奇,雪花生长形式在数学上很容易处理,并且已经由PI模拟,并且为酵母开发的广泛的生物信息学和分子遗传学工具允许合成构建具有精确定义的特性的多细胞菌株。
英文摘要
How did complex multicellular life arise from the single-celled microorganisms that defined life on Earth for billions of years? The rise of multicellular organisms drove a profound diversification of life that fundamentally changed Earth's ecology, yet little is known about how this major evolutionary transition occurred. This is largely due to the fact that most multicellular lineages are ancient, and early steps in this transition have been obscured by extinction. The PIs have overcome this limitation by developing a novel laboratory system, experimentally evolving simple multicellularity in Baker's yeast. Over thousands of generations of laboratory evolution, these cluster-forming 'snowflake yeast' evolve a suite of multicellular adaptations, including larger cluster size, an elevated rate of programmed cell death, and a more hydrodynamic profile. The PIs will use this model system to examine how novel multicellular traits arise in evolution, and will determine whether a fundamental developmental mechanism, the single-celled bottleneck that most multicellular organisms pass through (e.g., a single fertilized egg), improves the ability of natural selection to act on these emergent multicellular traits. This interdisciplinary work utilizes cutting-edge techniques in experimental evolution, next generation sequencing, molecular genetics, confocal microscopy, image analysis, and mathematical modeling. By illuminating the earliest steps in the evolutionary transition to multicellularity, the proposed research will help resolve an outstanding problem of central importance to biology. The evolution of biological complexity remains challenging to teach, particularly at the high school level. This award will support the development of a novel lab module, suitable for both high school and college classes, in which students use snowflake yeast and computer simulations to examine the evolution of multicellularity. The PIs will hold summer on-campus workshops to train teachers in the Atlanta area to use this curricula.Recent experiments have shown that unicellular organisms readily evolve to form multi-celled clusters, but little is known about how cellular clusters subsequently evolve greater multicellular complexity. The proposed research addresses this subject directly by asking the following questions: How do multicellular traits arise in evolution when mutation and recombination can only directly affect cell-level phenotype? Can early developmental mechanisms evolve to facilitate selection on these emergent multicellular traits? How are genes recruited for developmental functionality, and how are novel multicellular adaptations integrated into overall organism form and function? Answering the above questions will provide fundamental insight into the evolutionary origins of multicellular complexity, and will provide a theoretical foundation for similar investigations in other major evolutionary transitions. Snowflake yeast are an ideal experimental system for this work: the PIs have already evolved substantial morphological novelty, the snowflake growth form is mathematically tractable and has already been modeled by the PIs, and the extensive bioinformatic and molecular genetic tools developed for yeast allows for synthetic construction of multicellular strains with precisely defined properties.
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Nascent life cycles and the emergence of higher-level individuality
新生的生命周期和更高层次个性的出现
DOI:
10.1098/rstb.2016.0420
发表时间:
2017
期刊:
Philosophical Transactions of the Royal Society B: Biological Sciences
影响因子:
--
作者:
[Ratcliff, William C., Herron, Matthew, Conlin, Peter L., Libby, Eric]
通讯作者:
Libby, Eric
Ecological Advantages and Evolutionary Limitations of Aggregative Multicellular Development
集体多细胞发育的生态优势和进化限制
DOI:
10.1016/j.cub.2020.08.006
发表时间:
2020
期刊:
Current Biology
影响因子:
9.2
作者:
[Pentz, Jennifer T., Márquez-Zacarías, Pedro, Bozdag, G. Ozan, Burnetti, Anthony, Yunker, Peter J., Libby, Eric, Ratcliff, William C.]
通讯作者:
Ratcliff, William C.
Trait heritability in major transitions
重大转变中的性状遗传力
DOI:
10.1186/s12915-018-0612-6
发表时间:
2018
期刊:
BMC Biology
影响因子:
5.4
作者:
[Herron, Matthew D., Zamani-Dahaj, Seyed A., Ratcliff, William C.]
通讯作者:
Ratcliff, William C.
DOI:
10.1073/pnas.1813801116
发表时间:
2018-08
期刊:
Proceedings of the National Academy of Sciences
影响因子:
--
作者:
[Jonathan Michel;P. Yunker]
通讯作者:
Jonathan Michel;P. Yunker
Shortsighted Evolution Constrains the Efficacy of Long-Term Bet Hedging
短视的进化限制了长期赌注对冲的功效
DOI:
10.1086/701786
发表时间:
2019
期刊:
The American Naturalist
影响因子:
--
作者:
[Libby, Eric, Ratcliff, William C.]
通讯作者:
Ratcliff, William C.
共 6 条
Collaborative Research: BEE: A dormancy refuge in host-parasite eco-evolutionary dynamics
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项目类别:Standard Grant
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负责人:William Ratcliff
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依托单位:
CAREER: Examining the Role of Nascent Multicellular Life Cycles on the Evolution of Organismal Complexity
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负责人:William Ratcliff
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批准号:1456652
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资助金额:$27.51万
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财政年份:2015
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负责人:William Ratcliff
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依托单位:
国内基金
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