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PHA-1分析显示其在咽部发育中作用有限,而在其他组织中具有新功能。

Analysis of PHA-1 reveals a limited role in pharyngeal development and novel functions in other tissues.

作者信息

Kuzmanov Aleksandra, Yochem John, Fay David S

机构信息

Department of Molecular Biology, College of Agriculture and Natural Resources, University of Wyoming, Laramie, Wyoming 82071.

Department of Molecular Biology, College of Agriculture and Natural Resources, University of Wyoming, Laramie, Wyoming 82071

出版信息

Genetics. 2014 Sep;198(1):259-68. doi: 10.1534/genetics.114.166876. Epub 2014 Jul 9.

DOI:10.1534/genetics.114.166876
PMID:25009149
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4174937/
Abstract

PHA-1 encodes a cytoplasmic protein that is required for embryonic morphogenesis and attachment of the foregut (pharynx) to the mouth (buccal capsule). Previous reports have in some cases suggested that PHA-1 is essential for the differentiation of most or all pharyngeal cell types. By performing mosaic analysis with a recently acquired pha-1 null mutation (tm3671), we found that PHA-1 is not required within most or all pharyngeal cells for their proper specification, differentiation, or function. Rather, our evidence suggests that PHA-1 acts in the arcade or anterior epithelial cells of the pharynx to promote attachment of the pharynx to the future buccal capsule. In addition, PHA-1 appears to be required in the epidermis for embryonic morphogenesis, in the excretory system for osmoregulation, and in the somatic gonad for normal ovulation and fertility. PHA-1 activity is also required within at least a subset of intestinal cells for viability. To better understand the role of PHA-1 in the epidermis, we analyzed several apical junction markers in pha-1(tm3671) homozygous embryos. PHA-1 regulates the expression of several components of two apical junction complexes including AJM-1-DLG-1/discs large complex and the classical cadherin-catenin complex, which may account for the role of PHA-1 in embryonic morphogenesis.

摘要

PHA-1编码一种细胞质蛋白,该蛋白是胚胎形态发生以及前肠(咽)与口(颊囊)附着所必需的。先前的报道在某些情况下表明,PHA-1对大多数或所有咽细胞类型的分化至关重要。通过利用最近获得的pha-1无效突变(tm3671)进行镶嵌分析,我们发现大多数或所有咽细胞在其正常的特化、分化或功能过程中并不需要PHA-1。相反,我们的证据表明,PHA-1在咽的拱廊或前上皮细胞中起作用,以促进咽与未来颊囊的附着。此外,在胚胎形态发生过程中,表皮似乎需要PHA-1;在渗透调节过程中,排泄系统需要PHA-1;在正常排卵和生育过程中,体细胞性腺需要PHA-1。为了更好地理解PHA-1在表皮中的作用,我们分析了pha-1(tm3671)纯合胚胎中的几种顶端连接标记物。PHA-1调节两种顶端连接复合体的几个成分的表达,包括AJM-1-DLG-1/盘状大复合体和经典钙黏蛋白-连环蛋白复合体,这可能解释了PHA-1在胚胎形态发生中的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d428/4174937/7eb8a142b18d/259fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d428/4174937/90ca57bf5cb4/259fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d428/4174937/69bd7ecef9f1/259fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d428/4174937/7c14b57d1492/259fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d428/4174937/4ec9baa40e1e/259fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d428/4174937/7eb8a142b18d/259fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d428/4174937/90ca57bf5cb4/259fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d428/4174937/69bd7ecef9f1/259fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d428/4174937/7c14b57d1492/259fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d428/4174937/4ec9baa40e1e/259fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d428/4174937/7eb8a142b18d/259fig5.jpg

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本文引用的文献

1
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Genetics. 2014 Jan;196(1):211-23. doi: 10.1534/genetics.113.158485. Epub 2013 Nov 8.
2
From tissue mechanics to transcription factors.从组织力学到转录因子。
Differentiation. 2013 Oct;86(3):112-20. doi: 10.1016/j.diff.2013.07.004. Epub 2013 Aug 20.
3
The mechanical control of nervous system development.神经系统发育的机械控制。
PLoS Genet. 2019 Sep 16;15(9):e1008338. doi: 10.1371/journal.pgen.1008338. eCollection 2019 Sep.
4
Temporal regulation of epithelium formation mediated by FoxA, MKLP1, MgcRacGAP, and PAR-6.由FoxA、MKLP1、MgcRacGAP和PAR-6介导的上皮形成的时间调控。
Mol Biol Cell. 2017 Jul 15;28(15):2042-2065. doi: 10.1091/mbc.E16-09-0644. Epub 2017 May 24.
5
A maternal-effect selfish genetic element in .一种母体效应自私遗传元件在……中
Science. 2017 Jun 9;356(6342):1051-1055. doi: 10.1126/science.aan0621. Epub 2017 May 11.
6
FBN-1, a fibrillin-related protein, is required for resistance of the epidermis to mechanical deformation during C. elegans embryogenesis.FBN-1是一种与原纤蛋白相关的蛋白质,在秀丽隐杆线虫胚胎发育过程中,表皮对机械变形的抵抗需要该蛋白质。
Elife. 2015 Mar 23;4:e06565. doi: 10.7554/eLife.06565.
Development. 2013 Aug;140(15):3069-77. doi: 10.1242/dev.079145.
4
A genome-scale resource for in vivo tag-based protein function exploration in C. elegans.基于标签的线虫体内蛋白质功能探测的全基因组资源。
Cell. 2012 Aug 17;150(4):855-66. doi: 10.1016/j.cell.2012.08.001.
5
Mechanosensitive mechanisms in transcriptional regulation.机械敏感性机制在转录调控中的作用。
J Cell Sci. 2012 Jul 1;125(Pt 13):3061-73. doi: 10.1242/jcs.093005. Epub 2012 Jul 13.
6
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7
Multiple phenotypes resulting from a mutagenesis screen for pharynx muscle mutations in Caenorhabditis elegans.在秀丽隐杆线虫的咽肌突变诱变筛选中产生的多种表型。
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8
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9
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10
The molecular basis of organ formation: insights from the C. elegans foregut.器官形成的分子基础:来自秀丽隐杆线虫前肠的见解。
Annu Rev Cell Dev Biol. 2009;25:597-628. doi: 10.1146/annurev.cellbio.24.110707.175411.