Kamsteeg EJ, Bichet DG, Konings IB, Nivet H, Lonergan M, Arthus MF, van Os CH, Deen PM.

	Figure 1. Segregation of autosomal dominant NDI within the studied family. Healthy (open symbols) and affected (filled symbols) individuals, and male (squares) and females (circles) are indicated. The 12q13 haplotype is represented using the marker order: centromere-AFM259vf9-AQP2-D12S131-AFMb007yg5-telomere. The lengths of simple sequence tags in nucleotides (AFM259vf9 [1:313; 2:315], D12S131 [3:156; 4:158], AFMb007yg5 [b:226; d:230; j:242]), the C or T polymorphism in exon 2, 779-780insA nucleotide insertion (i) or normal sequence (n), and the A or C polymorphism in the 3′ UTR of AQP2 are indicated.
	Figure 2. COOH termini of wt-AQP2 and AQP2-insA. The COOH-terminal amino acids (one-letter symbols) and corresponding nucleotide sequences of wild-type aquaporin-2 (wt-AQP2) and AQP2-insA are shown, starting at aa 253. The c779-780insA and c836A>C mutations, identified in the mutant AQP2 allele of the patient, are underlined and bold. An asterisk indicates a stop codon.
	Figure 3. Expression of AQP2-insA in oocytes. (A) Water permeabilities. Oocytes were not injected (control), or injected with the indicated amounts of cRNA encoding wild-type AQP2 (wt-AQP2), AQP2-insA, AQP2-insA-R273* (insA-R273*), or AQP2-insA-G268* (insA-G268*). 2 d after injection, the mean water permeability (Pf ± SEM [in μm/s]; n >12) was determined in a standard swelling assay. (B) AQP2 protein expression levels. Total membranes (TM) and plasma membranes (PM) of oocytes that were used for the Pf measurements were isolated, and equivalents of four oocytes were immunoblotted. To allow comparison of AQP2 protein amounts, the membranes were incubated with AQP2 antibodies that were completely preabsorbed with a synthetic peptide raised against the last 15 amino acids of wt-AQP2 (not depicted). Complex glycosylated and nonglycosylated AQP2 proteins are indicated by c-AQP2 and AQP2, respectively. (C) Subcellular localization of AQP2-insA proteins. 2 d after injection, noninjected oocytes (control) and oocytes injected with 0.3 ng cRNA encoding the indicated AQP2 proteins were fixed and embedded in paraffin. On 5-μm sections, AQP2 was visualized using rabbit AQP2 antibodies, followed by Alexa® 594–conjugated anti–rabbit IgGs. Arrows indicate the plasma membrane.
	Figure 4. Localization of AQP2-insA in MDCK cells. MDCK cells expressing AQP2-insA (A) or wt-AQP2 (B) were grown to confluence, incubated without (control) or with forskolin, fixed, and immunostained using guinea pig AQP2-insA antibodies followed by an incubation with Alexa® 594–conjugated anti–guinea pig IgGs (red) or rabbit AQP2 antibodies, followed by Alexa® 488–conjugated anti–rabbit IgGs (green). The basolateral marker protein E-cadherin was visualized using specific rat antibodies followed by Cy5-conjugated anti–rat IgGs. Horizontal (XY) and vertical (XZ) images for AQP2-insA, wt-AQP2, and E-cadherin were obtained with a confocal laser-scanning microscope and merged (merge).
	Figure 5. Oligomerization state of AQP2-insA. (A) Homotetramerization. Membranes of MDCK cells expressing the indicated AQP2 proteins were dissolved in deoxycholate and subjected to differential velocity centrifugation. Fractions were collected from the top, of which fractions B–P were immunoblotted for AQP2. The fractions with peak intensities of the marker proteins ovalbumin (3.6 s), BSA (4.3 s), phosphorylase B (5.2 s), yeast alcohol dehydrogenase (7.4 s), and catalase (11.2 s) are indicated by arrows and by their sedimentation values. The molecular masses (in kD) of the respective AQP2 proteins are indicated on the left. (B) Heteroligomerization of AQP2-insA with wt-AQP2. Membranes of MDCK cells expressing wt-AQP2 (wt), AQP2-insA (insA), or VSV-G-tagged AQP2-insA together with wt-AQP2 (V-insA + wt) were solubilized in deoxycholate and centrifuged to remove nonsolubilized material. The supernatants were directly subjected to immunoblotting (TM, total membranes) or subjected to immunoprecipitation with affinity-purified AQP2-insA antibodies (insA IPs), followed by immunoblotting. Transferred AQP2 proteins were detected with rabbit AQP2 antibodies that recognize wt-AQP2 and AQP2-insA, or with affinity-purified rabbit AQP2 COOH-terminal antibodies (AQP2 C-term antibodies) that do not recognize AQP2-insA. Specific bands for VSV-G–tagged AQP2-insA (V-insA) and untagged AQP2 proteins (AQP2) are indicated on the right.
	Figure 6. Colocalization and regulation of AQP2-insA and wt-AQP2 in MDCK cells. (A) MDCK cells coexpressing wt-AQP2 and VSV-G–tagged AQP2-insA were incubated without (control) or with forskolin, fixed, and incubated with rabbit AQP2 COOH-terminal antibodies and guinea pig AQP2-insA antibodies, followed by Alexa® 488–conjugated anti–rabbit IgGs (green) and Alexa® 594–conjugated anti–guinea pig IgGs (red). Horizontal (XY) and vertical (XZ) images for wt-AQP2 and VSV-G–tagged AQP2-insA (V-AQP2-insA) were obtained with a confocal laser-scanning microscope and merged (merge). (B) MDCK cells heterologously expressing wt-AQP2 were supertransfected with a plasmid encoding GFP-tagged AQP2-R187C, and GFP-positive cells were selected using FACS® analysis. These pooled cells were grown to confluence on filter supports, treated as under A, and incubated with rabbit AQP2 COOH-terminal antibodies that recognize both wt-AQP2 and AQP2-R187C (wt-AQP2 + G-AQP2-R187C), followed by Alexa® 594–conjugated anti–rabbit IgGs (shown in green pseudocolor). The GFP signal of AQP2-R187C (G-AQP2-R187C) is given the red pseudocolor. Horizontal (XY) and vertical (XZ) images for were obtained with a confocal laser-scanning microscope and merged (merge).
	Figure 7. Subcellular localization of AQP2-insA mutants in MDCK cells. (A) MDCK cells stably expressing AQP2-S261* (wt-S261*) or AQP2-insA mutants (indicated by insA or introduced mutations; asterisks indicate stop codons) were incubated without (control) or with forskolin, fixed, and immunostained for AQP2 proteins using rabbit AQP2 and Alexa® 594–conjugated anti–rabbit antibodies. XZ images were made with a confocal laser-scanning microscope. (B) Mean values of integrated OD of surface or intracellular staining of AQP2 proteins were obtained from confocal laser-scanning microscope images. The ratio between surface and intracellular expression (ratio surface/intracellular ± SEM; n > 8) is determined from these values. Gray bars indicate this ratio from untreated cells, total bars indicate this ratio after forskolin stimulation.

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