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Mechanisms of growth and patterning of the mollusc shell

Mechanisms of growth and patterning of the mollusc shell
软体动物壳的生长和图案形成机制
批准号:
1656558
负责人:
J. David Lambert
金额:
$67.0万
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:
2017-04-01 至 2021-07-31

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中文摘要
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英文摘要
Molluscs are among the most successful animal groups, due in part to their strong and durable shells. Within a single group of molluscs, the snails, there is an enormous variety of different shell shapes, but all are variations on the same geometry, the helical spiral. Because of this underlying simplicity, snail shells are an important model for understanding how new biological structures are formed, but the cellular and developmental mechanisms that generate the shell are unknown. These researchers examined the patterns of cell division in the tissue that secretes the shell, and discovered two distinct growth zones. Remarkably, each zone displays cell division patterns that can explain the growth that drives shell shape. The researchers also found surprising fine-scale patterns in cell shape and gene activity that cause shell formation. The researchers will test the ability of these genes to form shells, and examine these patterns in another species with different shell coiling. Since snail shells are a familiar example of the great diversity of life, this work will provide an excellent example of the ways that small differences in genes and cells can create new and different shapes. The project will also enhance training of graduate and undergraduate students, and will create two classroom modules about shell shape to be used for outreach to middle school and high school students in a local high-poverty district.This project contains three aims to investigate the ability of cell division and gene expression to pattern the helically coiled secreted shells of the snail Ilyanassa. First, the researchers will define patterns of cell division that putatively contribute to shell shape, then functionally test several signaling pathways that may drive these patterns. Cell division will then be tested in another snail, Lymnaea stagnalis, to determine if the cell division patterns are conserved, and if strains with opposite coiling chirality have asymmetric division patterns correlated with the direction of shell coiling. The second aim will discover new candidate regulators of growth, patterning, and mineralization, via sequencing transcriptomes of embryos where shell development has been specifically blocked by cell ablation. Differentially regulated transcripts will be examined by in situ hybridization to validate their expression in the mantle edge. Preliminary data suggests that this aim will reveal intricate spatial patterning of the mantle edge, and recover new genes that might be regulating growth and patterning. Finally, specific gene-knockdown techniques will test the function of putative regulatory factors and mineralization genes. Preliminary results indicate that they can perturb both shell production and shell morphology. This project will provide fundamental insights into the mechanisms that generate the molluscan shell, and provide a cellular-level system for evaluating hypotheses related to mathematical modeling of morphology. The project is also expected to integrate knowledge of biomineralization with developmental biology.
期刊论文(6)
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会议论文
DOI: 10.1016/j.semcdb.2022.05.025
发表时间: 2022-05
期刊: Seminars in cell & developmental biology
影响因子: 7.3
作者: [Longjun Wu;J. Lambert]
通讯作者: Longjun Wu;J. Lambert
DOI: 10.1073/pnas.1816089116
发表时间: 2019-04-02
期刊: PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
影响因子: 11.1
作者: [Johnson, Adam B., Fogel, Nina S., Lambert, J. David]
通讯作者: Lambert, J. David
Genes with spiralian-specific protein motifs are expressed in spiralian ciliary bands
具有螺旋状特异性蛋白质基序的基因在螺旋状睫状带中表达
DOI: 10.1038/s41467-020-17780-7
发表时间: 2020
期刊: Nature Communications
影响因子: 16.6
作者: [Wu, Longjun, Hiebert, Laurel S., Klann, Marleen, Passamaneck, Yale, Bastin, Benjamin R., Schneider, Stephan Q., Martindale, Mark Q., Seaver, Elaine C., Maslakova, Svetlana A., Lambert, J. David]
通讯作者: Lambert, J. David
A serpin is required for ectomesoderm, a hallmark of spiralian development
外中胚层需要丝氨酸蛋白酶抑制剂,这是螺旋发育的标志
DOI: 10.1016/j.ydbio.2020.10.011
发表时间: 2021
期刊: Developmental Biology
影响因子: 2.7
作者: [Wu, Longjun, Lambert, J. David]
通讯作者: Lambert, J. David
The evolution of retinoic acid signaling in animals: functional insights from a mollusc embryo
  • 批准号:
    2053371
  • 项目类别:
    Continuing Grant
  • 资助金额:
    $65.0万
  • 财政年份:
    2021
  • 负责人:
    J. David Lambert
  • 依托单位:
Dpp/BMP2-4 signaling in a spiralian embryo
  • 批准号:
    1146782
  • 项目类别:
    Continuing Grant
  • 资助金额:
    $55.14万
  • 财政年份:
    2012
  • 负责人:
    J. David Lambert
  • 依托单位:
Patterning the Micromeres in the Spiralian Blastula
  • 批准号:
    0844734
  • 项目类别:
    Standard Grant
  • 资助金额:
    $51.0万
  • 财政年份:
    2009
  • 负责人:
    J. David Lambert
  • 依托单位:
Centrosomal mRNAs in Asymmetric Cell Division
  • 批准号:
    0544220
  • 项目类别:
    Standard Grant
  • 资助金额:
    $40.0万
  • 财政年份:
    2006
  • 负责人:
    J. David Lambert
  • 依托单位:
国内基金
海外基金
基于FP-Growth关联分析算法的重症患者抗菌药物精准决策模型的构建和实证研究
  • 批准号:
    2024Y9049
  • 项目类别:
    省市级项目
  • 资助金额:
    100.0万元
  • 批准年份:
    2024
  • 负责人:
    阮君山
  • 依托单位:
含Re、Ru先进镍基单晶高温合金中TCP相成核—生长机理的原位动态研究
  • 批准号:
    52301178
  • 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:
    夏万顺
  • 依托单位:
新型小分子蛋白—人肝细胞生长因子三环域(hHGFK1)抑制破骨细胞及治疗小鼠骨质疏松的疗效评估与机制研究
  • 批准号:
    82370885
  • 项目类别:
    面上项目
  • 资助金额:
    49.00万元
  • 批准年份:
    2023
  • 负责人:
    姚晨
  • 依托单位:
基于 Klotho 调控 FGF23/SGK1/NF-κB信号通路研究糖尿病肾病血管钙化机制及肾元颗粒干预作用
  • 批准号:
  • 项目类别:
    省市级项目
  • 资助金额:
    --
  • 批准年份:
    2022
  • 负责人:
  • 依托单位: