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:
1656849
负责人:
Eric Libby
金额:
$12.12万
依托单位:
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 2022-01-31
中文摘要
复杂的多细胞生命是如何从数十亿年来定义地球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。这在很大程度上是由于大多数多细胞谱系是古老的,这种转变的早期步骤已经被灭绝所掩盖。PI通过开发一种新的实验室系统,在面包酵母中实验性地进化简单的多细胞性,克服了这一限制。经过数千代的实验室进化,这些成簇的“雪花酵母”进化出了一系列多细胞适应,包括更大的簇大小、更高的程序性细胞死亡率以及更具流体动力学特征。PI将使用这个模型系统来研究新的多细胞性状是如何在进化中出现的,并将确定一个基本的发育机制,即大多数多细胞生物所通过的单细胞瓶颈(例如,单个受精卵),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。通过阐明多细胞生物进化过渡的最早阶段,这项研究将有助于解决生物学中一个重要的突出问题。生物复杂性的进化仍然是具有挑战性的教学,特别是在高中水平。该奖项将支持开发一种新的实验室模块,适用于高中和大学课程,学生使用雪花酵母和计算机模拟来研究多细胞的进化。PI将举办夏季校园研讨会,培训亚特兰大地区的教师使用这门课程。最近的实验表明,单细胞生物很容易进化形成多细胞簇,但对细胞簇如何随后进化出更大的多细胞复杂性知之甚少。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,多细胞性状是如何在进化中出现的?早期的发育机制能否进化以促进对这些新出现的多细胞性状的选择?基因是如何为发育功能而募集的,新的多细胞适应是如何整合到整个生物体的形式和功能中的?对上述问题的研究将为多细胞复杂性的进化起源提供基本的见解,并将为其他主要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学新奇,雪花生长形式在数学上是易于处理的,并且已经被PI建模,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具有精确定义的特性的多细胞菌株的合成构建。
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.
期刊论文(6)
专著(0)
科研奖励(0)
会议论文
登录
查看更多内容
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.
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.
DOI:
10.1017/s0024282921000256
发表时间:
2021-07
期刊:
The Lichenologist
影响因子:
--
作者:
[E. Libby;W. Ratcliff]
通讯作者:
E. Libby;W. Ratcliff
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
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:
Cell Research
-
批准号:31224802
-
项目类别:专项基金项目
-
资助金额:24.0万元
-
批准年份:2012
-
负责人:程磊
-
依托单位:
Cell Research
-
批准号:31024804
-
项目类别:专项基金项目
-
资助金额:24.0万元
-
批准年份:2010
-
负责人:程磊
-
依托单位:
Cell Research (细胞研究)
-
批准号:30824808
-
项目类别:专项基金项目
-
资助金额:24.0万元
-
批准年份:2008
-
负责人:张爱兰
-
依托单位:
Research on the Rapid Growth Mechanism of KDP Crystal
-
批准号:10774081
-
项目类别:面上项目
-
资助金额:45.0万元
-
批准年份:2007
-
负责人:滕冰
-
依托单位: