scholarly journals Isoform-specific roles of the Drosophila filamin-type protein Jitterbug (Jbug) during development

Genetics ◽  
2021 ◽  
Author(s):  
SeYeon Chung ◽  
Thao Phuong Le ◽  
Vishakha Vishwakarma ◽  
Yim Ling Cheng ◽  
Deborah J Andrew

Abstract Filamins are highly conserved actin-crosslinking proteins that regulate organization of the actin cytoskeleton. As key components of versatile signaling scaffolds, filamins are implicated in developmental anomalies and cancer. Multiple isoforms of filamins exist, raising the possibility of distinct functions for each isoform during development and in disease. Here, we provide an initial characterization of jitterbug (jbug), which encodes one of the two filamin-type proteins in Drosophila. We generate Jbug antiserum that recognizes all of the spliced forms and reveals differential expression of different Jbug isoforms during development, and a significant maternal contribution of Jbug protein. To reveal the function of Jbug isoforms, we create new genetic tools, including a null allele that deletes all isoforms, hypomorphic alleles that affect only a subset, and UAS lines for Gal4-driven expression of the major isoforms. Using these tools, we demonstrate that Jbug is required for viability and that specific isoforms are required in the formation of actin-rich protrusions including thoracic bristles in adults and ventral denticles in the embryo. We also show that specific isoforms of Jbug show differential localization within epithelia and that maternal and zygotic loss of jbug disrupts Crumbs (Crb) localization in several epithelial cell types.

2020 ◽  
Author(s):  
SeYeon Chung ◽  
Thao Phuong Le ◽  
Vishakha Vishwakarma ◽  
Yim Ling Cheng ◽  
Deborah J. Andrew

ABSTRACTFilamins are highly conserved actin-crosslinking proteins that regulate organization of the actin cytoskeleton. As key components of versatile signaling scaffolding complexes, filamins are implicated in developmental anomalies and cancer. Multiple isoforms of filamins exist, raising the possibility of distinct functions of each isoform during development and in diseases. Here, we provide an initial characterization of jitterbug (jbug), which encodes one of the two filamin-type genes in Drosophila. We generate Jbug antiserum that recognizes all of the spliced forms, which reveals differential expression of different Jbug isoforms during development with a significant maternal contribution of Jbug protein. To reveal the function of Jbug isoforms, we create new genetic tools, including a null allele that deletes all isoforms, hypomorphic alleles that affect only a subset, and UAS lines for expression of the major isoforms. Using these tools, we demonstrate that Jbug is required for viability and that specific isoforms of Jbug are required in the formation of actin-rich protrusions such as thoracic bristles in adults and ventral denticles in the embryo. We also provide evidence for trans-splicing in the jbug locus.


2019 ◽  
Vol 17 (7) ◽  
pp. 1556-1570 ◽  
Author(s):  
Mayuri Prasad ◽  
Brijesh Kumar ◽  
Poornima Bhat-Nakshatri ◽  
Manjushree Anjanappa ◽  
George Sandusky ◽  
...  

Author(s):  
G.M. Vernon ◽  
A. Surace ◽  
R. Witkus

The hepatopancreas consists of a pair of bilobed tubules comprised of two epithelial cell types. S cells are absorptive and accumulate metals such as copper and zinc. Ca++ concentrations vary between the S and B cells and during the molt cycle. Roer and Dillaman implicated Ca++-ATPase in calcium transport during molting in Carcinus maenas. This study was undertaken to compare the localization of Ca++-ATPase activity in the S and B cells during intermolt.


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