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WormBase Tree Display for Expr_pattern: Expr2621

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Name Class

Expr2621Expression_ofGeneWBGene00002248
Reflects_endogenous_expression_ofWBGene00002248
Expression_dataLife_stageWBls:0000024
WBls:0000038
WBls:0000027
WBls:0000035
WBls:0000041
WBls:0000015
WBls:0000021
WBls:0000010
WBls:0000013
Anatomy_termWBbt:0003675Partial
WBbt:0003681Certain
WBbt:0005319Certain
WBbt:0005767Certain
WBbt:0005772Certain
WBbt:0005775Certain
WBbt:0005829Partial
WBbt:0006749Certain
GO_termGO:0005604
Subcellular_localizationIn nid-1(ur41) animals, lam-3 is localized with the mispositioned axons rather than along the normal nerve pathways. This suggests that lam-3 is localized to neuronal cell surfaces by specific lam-3 receptors.
TypeAntibodyRabbit and chicken polyclonal antibody. To generate antisera against LAM-3, a plasmid construct was made by subcloning into the vector pQE (Qiagen, CA) an 800 bp cDNA fragment that contains the sequence encoding the G3 domain. The fusion protein produced contain 6HIS-tags and were purified according to the instructions of Qiagen and were used to immunize rabbits. Antisera against each fusion protein were also raised in Chicken.
PatternThe antisera indicate that early expression occurs during gastrulation.
lam-3 is also associated with the nervous system. During elongation and throughout the rest of development, lam-3 is localized at the nerve ring, at the right fascicle of the ventral nerve cord and at the sublateral nerves.
lam-3 is first detected between tissue layers near the end of gastrulation and then becomes localized along the muscle cells as the embryo begins to elongate. By the 3-fold stage of elongation, staining along the muscle quadrants is weaker and becomes restricted to a band at the center of each quadrant, which colocalizes with the dorsal and ventral sublateral nerve tracts in the adult. Staining is intense around the pharynx, pharyngeal-intestinal valve, and intestine during morphogenesis. In larvae and adults, the antiserum stains the spermatheca strongly and only weakly stains the pharynx, the intestine and the excretory canal.
PictureWBPicture0000007556
WBPicture0000007559
RemarkColocalization Assay: In order to compare directly the distribution of lam-3 and epi-1, both subunits were co-stained using species-specific secondary antibody conjugates. As the germ layers develop, both subunits are deposited between the layers. However, the staining for laminin A is most intense around the pharyngeal and intestinal precursor cells, whereas staining for laminin B is most intense around the myoblast cells and along epidermal cells. By the onset of elongation, distinct layers of laminin A and laminin B staining can be distinguished, particularly anteriorly between the developing pharynx and the body wall. This indicates that the segregation of the laminin isoforms begins early, before or as organogenesis proceeds. In mnDf90, the two subunits remain differentially localized after elongation. lam-3 is localized to the pharyngeal basement membrane, whereas epi-1 is associated mainly with the body wall basement membranes and only weakly with the pharyngeal basement membrane. These results indicate that each laminin alpha subunit is segregated in the embryo to different adjacent basement membranes and that each membrane retains its unique subunit composition.
ReferenceWBPaper00006014
Antibody_infoWBAntibody00000660
WBAntibody00000661