Mechanisms of specification, quiescence, and regeneration of primordial germ cells
原始生殖细胞的规范、静止和再生机制
基本信息
- 批准号:10725044
- 负责人:
- 金额:$ 4.16万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2021
- 资助国家:美国
- 起止时间:2021-06-01 至 2026-05-31
- 项目状态:未结题
- 来源:
- 关键词:AdultAnimalsBiochemicalBiologicalBiologyBiomedical ResearchCRISPR/Cas technologyCell LineageCell TransplantationCellsCellular biologyCharacteristicsChordataComplexCoupledDevelopmentDropsEchinodermataEmbryoEmbryonic DevelopmentEvaluationEventFemaleGene ExpressionGenesGenomicsGerm CellsGerm LinesHeartInheritedKnowledgeMammalsManualsMetabolicModelingMolecularMorphologyNatural regenerationOligonucleotidesOrganismProcessReagentResolutionSea UrchinsSexual ReproductionSignal PathwaySignal TransductionSisterSpecific qualifier valueStarfishSterilityStructure of primordial sex cellSystemTechnologyTissue TransplantationTransplantationVertebratesVisualizationWorkanimal resourcechromatin modificationeggexpirationgenetic manipulationin vivoinnovationlongitudinal analysismRNA sequencingmalemodel organismoptical imagingoptogeneticsposttranscriptionalregenerative cellserial imagingsmall moleculesperm cellstem cellstrait
项目摘要
Project Summary
Sexual reproduction requires a germline, a lineage of cells formed in early embryos that ultimately
develops into eggs or sperm in the adult. Lore has it that when you lose your germline in development, you
become a sterile adult. In many animals, especially in the current favorites of lab animals, that is largely true.
We use “rule breakers” though and find such lore unfounded. Our work focuses on the biology of primordial
germ cells, how they form during early development, and how they regenerate when the originals are removed.
Our work leverages embryos from a sister group to chordates – the sea star and sea urchin. While not
common organisms for biomedical research, these echinoderms have many strategic benefits for revealing
unique perspectives in the biology of germline formation and regeneration. Millions of synchronous embryos
from a single male/female cross allow biochemical and metabolic analysis of the germline, the resultant
embryos have ideal transparency for in vivo longitudinal imaging, they develop rapidly, are easy to manipulate
(single cell drop-mRNA-seq, optogenetics, cell and tissue transplantations) and they are well suited to
complementary gene perturbation approaches (CRISPR/Cas9, morpholinoantisense oligonucleotides, MASO),
and small molecule perturbations. The existing deep genomic and reagent resources for these animals,
coupled with their tractable experimental characteristics, yields a unique system for understanding primordial
germ cell biology with defined molecular and morphological endpoints, in live embryos with longitudinal
analysis, distinct metrics of quantitation, and transgenerational evaluations.
We interrogate all levels of gene expression for this work, from chromatin modification to post-
transcriptional processing and post-translational networks, because that is what the embryos are “telling” us is
needed to understand these complex, and deeply rooted events in sexual reproduction. Our work emphasizes
longitudinal, in vivo analysis using high resolution optical imaging coupled with genomic perturbations, signal
pathway manipulations and manual transplantations and expirations to leverage contrasting mechanisms in
germ cell formation between closely related organisms. Sea urchins and sea stars have historically not been
genetically manipulated, and this reason is precisely how germ line regeneration has been discovered in this
and other animals seen to bear this trait. Relying on manual manipulations meant the genes needed for
regeneration were not disturbed, revealing their germ cell regenerative abilities. With new state-of-the-art
technologies, these animals can now be exploited with transgenerational analysis. Overall, our work
interrogates important biological questions from unique experimental perspectives using rule-breaking models
for innovation in the pursuit of new knowledge.
项目总结
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
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专利数量(0)
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GARY M WESSEL其他文献
GARY M WESSEL的其他文献
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{{ truncateString('GARY M WESSEL', 18)}}的其他基金
Mechanisms of specification, quiescence, and regeneration of primordial germ cells
原始生殖细胞的规范、静止和再生机制
- 批准号:
10797823 - 财政年份:2021
- 资助金额:
$ 4.16万 - 项目类别:
Mechanisms of specification, quiescence, and regeneration of primordial germ cells
原始生殖细胞的规范、静止和再生机制
- 批准号:
10624736 - 财政年份:2021
- 资助金额:
$ 4.16万 - 项目类别:
Mechanisms of specification, quiescence, and regeneration of primordial germ cells
原始生殖细胞的规范、静止和再生机制
- 批准号:
10472183 - 财政年份:2021
- 资助金额:
$ 4.16万 - 项目类别:
Mechanisms of specification, quiescence, and regeneration of primordial germ cells
原始生殖细胞的规范、静止和再生机制
- 批准号:
10397891 - 财政年份:2021
- 资助金额:
$ 4.16万 - 项目类别:
Mechanisms of specification, quiescence, and regeneration of primordial germ cells
原始生殖细胞的规范、静止和再生机制
- 批准号:
10414946 - 财政年份:2021
- 资助金额:
$ 4.16万 - 项目类别:
Mechanisms of specification, quiescence, and regeneration of primordial germ cells
原始生殖细胞的规范、静止和再生机制
- 批准号:
10631065 - 财政年份:2021
- 资助金额:
$ 4.16万 - 项目类别:
Sequential restriction of germ line progenitors by induction
通过诱导连续限制种系祖细胞
- 批准号:
9980947 - 财政年份:2019
- 资助金额:
$ 4.16万 - 项目类别:
2015 Fertilization and Activation of Development Gordon Research Conference & Gordon Research Seminar
2015年施肥与发育激活戈登研究会议
- 批准号:
8975378 - 财政年份:2015
- 资助金额:
$ 4.16万 - 项目类别:
Single Nucleotide Genome Modifications in Oocytes
卵母细胞中的单核苷酸基因组修饰
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8691207 - 财政年份:2014
- 资助金额:
$ 4.16万 - 项目类别:
Cell Surface Changes During the Egg-to-Embryo Transition
卵子到胚胎转变过程中细胞表面的变化
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8051018 - 财政年份:2010
- 资助金额:
$ 4.16万 - 项目类别:
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