Rap1小GTP酶在果蝇眼睛发育过程中影响细胞命运或存活和形态发生模式。

IF 2.2 3区 生物学 Q4 CELL BIOLOGY Differentiation Pub Date : 2023-09-01 DOI:10.1016/j.diff.2023.06.001
Philip P. Yost , Abdulqater Al-Nouman, Jennifer Curtiss
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引用次数: 0

摘要

黑腹果蝇的眼睛有助于确定细胞如何相互交流以确定细胞命运,以及细胞形态发生和模式形成。在这里,我们描述了小GTPase Rap1对黑腹果蝇眼睛多种细胞类型发育的影响。尽管Rap1先前与眼睛发育中的RTK-Ras-MAPK信号传导有关,但我们证明,在眼睛发育中细胞命运规范的几个事件中,Rap1活性的操纵通过Delta/Noch信号传导的增加或减少而改变。此外,我们证明,操纵Rap1在原代色素细胞或毫米间细胞中的功能会影响视锥细胞接触切换、原代色素上皮细胞包围小眼团以及第二和第三色素上皮细胞的分选。这些数据表明,Rap1在蛹期的小眼细胞募集/存活和小眼形态发生中都有作用。他们为未来关于Rap1在这些事件中的作用的实验奠定了基础。
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The Rap1 small GTPase affects cell fate or survival and morphogenetic patterning during Drosophila melanogaster eye development

The Drosophila melanogaster eye has been instrumental for determining both how cells communicate with one another to determine cell fate, as well as cell morphogenesis and patterning. Here, we describe the effects of the small GTPase Rap1 on the development of multiple cell types in the D. melanogaster eye. Although Rap1 has previously been linked to RTK-Ras-MAPK signaling in eye development, we demonstrate that manipulation of Rap1 activity is modified by increase or decrease of Delta/Notch signaling during several events of cell fate specification in eye development. In addition, we demonstrate that manipulating Rap1 function either in primary pigment cells or in interommatidial cells affects cone cell contact switching, primary pigment cell enwrapment of the ommatidial cluster, and sorting of secondary and tertiary pigment cells. These data suggest that Rap1 has roles in both ommatidial cell recruitment/survival and in ommatidial morphogenesis in the pupal stage. They lay groundwork for future experiments on the role of Rap1 in these events.

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来源期刊
Differentiation
Differentiation 生物-发育生物学
CiteScore
4.10
自引率
3.40%
发文量
38
审稿时长
51 days
期刊介绍: Differentiation is a multidisciplinary journal dealing with topics relating to cell differentiation, development, cellular structure and function, and cancer. Differentiation of eukaryotes at the molecular level and the use of transgenic and targeted mutagenesis approaches to problems of differentiation are of particular interest to the journal. The journal will publish full-length articles containing original work in any of these areas. We will also publish reviews and commentaries on topics of current interest. The principal subject areas the journal covers are: • embryonic patterning and organogenesis • human development and congenital malformation • mechanisms of cell lineage commitment • tissue homeostasis and oncogenic transformation • establishment of cellular polarity • stem cell differentiation • cell reprogramming mechanisms • stability of the differentiated state • cell and tissue interactions in vivo and in vitro • signal transduction pathways in development and differentiation • carcinogenesis and cancer • mechanisms involved in cell growth and division especially relating to cancer • differentiation in regeneration and ageing • therapeutic applications of differentiation processes.
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