Smith KM et al. (2002), The cysteine-rich domain regulates ADAM proteas...

XB-ART-6089

J Cell Biol 2002 Dec 09;1595:893-902. doi: 10.1083/jcb.200206023.

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The cysteine-rich domain regulates ADAM protease function in vivo.

Smith KM , Gaultier A , Cousin H , White JM , DeSimone DW .

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ADAMs are membrane-anchored proteases that regulate cell behavior by proteolytically modifying the cell surface and ECM. Like other membrane-anchored proteases, ADAMs contain candidate "adhesive" domains downstream of their metalloprotease domains. The mechanism by which membrane-anchored cell surface proteases utilize these putative adhesive domains to regulate protease function in vivo is not well understood. We address this important question by analyzing the relative contributions of downstream extracellular domains (disintegrin, cysteine rich, and EGF-like repeat) of the ADAM13 metalloprotease during Xenopus laevis development. When expressed in embryos, ADAM13 induces hyperplasia of the cement gland, whereas ADAM10 does not. Using chimeric constructs, we find that the metalloprotease domain of ADAM10 can substitute for that of ADAM13, but that specificity for cement gland expansion requires a downstream extracellular domain of ADAM13. Analysis of finer resolution chimeras indicates an essential role for the cysteine-rich domain and a supporting role for the disintegrin domain. These and other results reveal that the cysteine-rich domain of ADAM13 cooperates intramolecularly with the ADAM13 metalloprotease domain to regulate its function in vivo. Our findings thus provide the first evidence that a downstream extracellular adhesive domain plays an active role in regulating ADAM protease function in vivo. These findings are likely relevant to other membrane-anchored cell surface proteases.

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Species referenced: Xenopus laevis
Genes referenced: adam10 adam13 adam28.2 egf gnpda1 muc2 muc2l myc tbx2

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	Figure 3. Localization of ADAM13, ADAM10, and XCG mRNA in early Xenopus embryos. (A) In an anterior view at stage 16, ADAM13 (purple, black arrow) mRNA is found in the neural crest and just dorsal to the cement gland anlagen (as marked by XCG mRNA expression in red, arrowhead), but the two transcripts do not overlap. (B) ADAM10 (light purple, open arrow) mRNA is localized to the entire neural plate and placodes, and encompasses the expression field of XCG. No distinct red color revealing XCG mRNA expression is seen because it is overlaid by the light purple ADAM10 costaining. (C) In a schematic of the Xenopus embryo at stage 16, the pink represents the entire neural plate and surrounding placodal and cement gland anlagen that express ADAM10 mRNA (open arrow). The ADAM10-expressing area encompasses both the regions of ADAM13 mRNA expression (blue, black arrow) and XCG (red, arrowhead) (Nieuwkoop and Faber, 1994).
	Figure 4. Overexpression of wild-type ADAM13, but not ADAM10, results in hyperplasia of the cement gland. (A) Transcripts encoding ADAM constructs are microinjected into the animal pole of one blastomere at the two-cell stage. The embryos are allowed to recover until stage 22+, and then fixed for whole mount in situ hybridization with the cement gland marker XCG. (B) The increase in XCG mRNA levels caused by ADAM13 overexpression was quantified by RNA spot blot. Data are represented as relative values of expression based on average pixel densities obtained using the PhosphorImager. All levels of expression were within the linear range of this detection method. Data are shown as means Â± SD of five independent experiments, each with pooled RNAs from 10 embryos. By stage 17, a twofold increase in XCG mRNA levels (P < 0.05) was found in embryos expressing ADAM13, but not E/A ADAM13 or ADAM10. The differences in XCG mRNA levels quantified by RNA spot blot were also observed by whole mount in situ hybridization. (C) GFP-injected embryos had no alterations in the cement gland marker XCG (black arrow), whereas large, ectopic islands of XCG-positive cells (D, arrow) were found when overexpressing ADAM13. Expression of the E/A ADAM13 mutant (E) or ADAM10 (F) had no affect on cement gland formation. NI, noninjected control; E/A13, E/A ADAM13.
	Figure 7. Summary of ADAM10/13 construct expression in embryos. The molecular weights in kD were calculated by MacVector software and include the addition of the six myc tags and predicted N-linked glycosylations. After in situ hybridization with XCG, embryos were scored for mild or severe cement gland perturbations. The embryos with mild phenotypes were subdivided into two classes, in some cases (shown with a back slash), defined as one to three small spots of ectopic XCG expression or three to four small spots accompanied by <10% expansion of the area of the main cement gland. Severe phenotypes had numerous large islands of ectopic cement gland or substantial expansions (>10%) of the existing cement gland. Up arrows indicate the ability of a construct to induce severe cement gland hyperplasia (corresponding to arrows in Fig. 5). Constructs with high levels of cell surface expression in the met form (as compared with ADAM13) have two pluses (++) and embryos with lower levels of met forms are given one plus (+). N, the number of embryos assayed. aLow cell surface expression, but robust activity. *Previously we reported separate experiments involving the coexpression of equal amounts of transcript (0.5 ng each) encoding wild-type and E/A ADAM13, which led to a marked reduction (62%) in cement gland hyperplasia. We conclude that E/A ADAM13 can function as a dominant-negative inhibitor of wild-type ADAM13 in the cement gland assay; the details are reported in Alfandari et al. (2001).
	Figure 8. Anterior views of representative stage-22 Xenopus embryos showing XCG mRNA expression. (A) Embryos injected with GFP alone have no alterations in XCG expression. (B) Like ADAM13, the 10PM/13 chimeric construct causes a large expansion in XCG. The 10/13DCE (C) and 10/13DC (D) chimeras also perturb the cement gland. (E) An E/A point mutant in the catalytically active site of the 10/13DC chimera ablates its ability to cause hyperplasia of the cement gland. (F) Replacing ADAM13's disintegrin and cysteine-rich domains (chimera 13/10DC) did not fully ablate the XCG expansion, but it did lessen its severity. Replacing the disintegrin domain of ADAM13 with that of ADAM10 (chimera 13/10D) did not alter the function (G), whereas replacing only ADAM10's cysteine-rich domain with that of ADAM13 (10/13C) was sufficient to give that chimera the ability to cause alterations in XCG (H). Swapping ADAM13's cysteine-rich domain caused both a quantitative (6% severe phenotype vs. 33% for wild-type ADAM13; Fig. 7) and qualitative (I) decrease in activity. (J) Three point mutations in the disintegrin loop of ADAM13 diminish its ability to cause the enlargement of the cement gland, but do not affect its ability to cause its own degradation in vitro (unpublished data).
	Figure 1. Schematic representation of cell surface proteases. Each is anchored in the membrane with a transmembrane domain or GPI linker. MT-MMPs and ectopeptidases come in both types, whereas meprins and ADAMs both possess transmembrane domains and cytoplasmic tails of varying sizes. Some ADAMs have SH3 ligand domains within their cytoplasmic tails. The cytoplasmic tails of meprin Î² subunits have a PKC phosphorylation site.
	Figure 2. Sequence comparison of X-ADAM10 and X-ADAM13. Amino acid sequence alignments of full-length ADAM10 (GenBank/EMBL/DDBJ accession no. AF508151) and ADAM13 (accession no. U66003) with domain boundaries in black. The putative signal sequences are shown with an arrowhead. The cysteine-switch cysteine is indicated by a star (â) and all potential N-linked glycosylation sites in ADAM10 are denoted with an open arrow (â). The metalloprotease active site is underlined by a solid black line, the disintegrin loop is underlined by a broken line, and the transmembrane (TM) domain is underlined with a wavy line. All putative SH3 binding sites in the cytoplasmic tails of ADAMs 10 and 13 are boxed. Mutated amino acids in the zinc binding site (ADAM13 E341 to A; ADAM10 E385 to A) and the disintegrin loop (ADAM10 S529 to A and D530 to A; ADAM13 G474 to A, S475 to A, and D477 to A) are highlighted in bold.
	Figure 5. Schematic representation of ADAM10 and -13 constructs. Domains between ADAM10 (white) and ADAM13 (black) were switched as units (Pro/Met and DC Â± E) or as individual domains (D and C). Chimeras containing metalloprotease domains with the catalytically inactive E/A point mutation were made. Mutations were also made in the disintegrin loops of both ADAM10 and -13. All constructs have been myc tagged. Mutated domains are denoted by an X. ADAM constructs that cause severe hyperplasia of the cement gland when ectopically expressed are designated by an up arrow. Blank boxes in this chart indicate that the construct had no significant affect on the cement gland. Set A consists of the wild-type and E/A point mutant constructs of ADAM10 and -13. Chimeras are grouped into Set B, for pro and met domain swaps, and Set C, for disintegrin and cysteine-rich domain swaps. Set D groups the disintegrin loop alanine point mutations.
	Figure 6. All ADAM constructs are proteolytically processed and found on the cell surface. (A) In whole embryo lysate Western blots with the antiâmyc tag antibody, 9E10, both wild type and E/A mutants of ADAM10, ADAM13, and the Pro/Met chimeras are all found in unprocessed precursor forms with the pro-domain (black arrow) and in metalloprotease active forms, with the functionally repressive pro-domain removed (open arrows). (B and C) By affinity purification of cell surface biotin-labeled proteins and Western blotting with 9E10, the pro forms (black arrows) and metalloprotease forms (met forms, open arrows) of all ADAM constructs are seen. The pro and met forms generally run as expected based on calculated molecular weights with the addition of the myc tag.

References [+] :

Alfandari, Xenopus ADAM 13 is a metalloprotease required for cranial neural crest-cell migration. 2001, Pubmed, Xenbase