Charles R. Bronfman Institute for Personalized Medicine, and Department of Medicine, Mount Sinai School of Medicine, New York, New York.
Address correspondence to: Erwin P. Böttinger, Charles R. Bronfman Institute for Personalized Medicine, and Department of Medicine, Mount Sinai School of Medicine, One Gustave L. Levy Pl., Box 1003, New York, NY 10029. Phone: 212.241.0800; Fax: 212.849.2643; E-mail: firstname.lastname@example.org.
Published February 22, 2010 - More info
The autosomal recessive kidney disease nephronophthisis (NPHP) constitutes the most frequent genetic cause of terminal renal failure in the first 3 decades of life. Ten causative genes (NPHP1–NPHP9 and NPHP11), whose products localize to the primary cilia-centrosome complex, support the unifying concept that cystic kidney diseases are “ciliopathies”. Using genome-wide homozygosity mapping, we report here what we believe to be a new locus (NPHP-like 1 [NPHPL1]) for an NPHP-like nephropathy. In 2 families with an NPHP-like phenotype, we detected homozygous frameshift and splice-site mutations, respectively, in the X-prolyl aminopeptidase 3 (XPNPEP3) gene. In contrast to all known NPHP proteins, XPNPEP3 localizes to mitochondria of renal cells. However, in vivo analyses also revealed a likely cilia-related function; suppression of zebrafish xpnpep3 phenocopied the developmental phenotypes of ciliopathy morphants, and this effect was rescued by human XPNPEP3 that was devoid of a mitochondrial localization signal. Consistent with a role for XPNPEP3 in ciliary function, several ciliary cystogenic proteins were found to be XPNPEP3 substrates, for which resistance to N-terminal proline cleavage resulted in attenuated protein function in vivo in zebrafish. Our data highlight an emerging link between mitochondria and ciliary dysfunction, and suggest that further understanding the enzymatic activity and substrates of XPNPEP3 will illuminate novel cystogenic pathways.
John F. O’Toole, Yangjian Liu, Erica E. Davis, Christopher J. Westlake, Massimo Attanasio, Edgar A. Otto, Dominik Seelow, Gudrun Nurnberg, Christian Becker, Matti Nuutinen, Mikko Kärppä, Jaakko Ignatius, Johanna Uusimaa, Salla Pakanen, Elisa Jaakkola, Lambertus P. van den Heuvel, Henry Fehrenbach, Roger Wiggins, Meera Goyal, Weibin Zhou, Matthias T.F. Wolf, Eric Wise, Juliana Helou, Susan J. Allen, Carlos A. Murga-Zamalloa, Shazia Ashraf, Moumita Chaki, Saskia Heeringa, Gil Chernin, Bethan E. Hoskins, Hassan Chaib, Joseph Gleeson, Takehiro Kusakabe, Takako Suzuki, R. Elwyn Isaac, Lynne M. Quarmby, Bryan Tennant, Hisashi Fujioka, Hannu Tuominen, Ilmo Hassinen, Hellevi Lohi, Judith L. van Houten, Agnes Rotig, John A. Sayer, Boris Rolinski, Peter Freisinger, Sethu M. Madhavan, Martina Herzer, Florence Madignier, Holger Prokisch, Peter Nurnberg, Peter Jackson, Hemant Khanna, Nicholas Katsanis, Friedhelm Hildebrandt
While erudite cell biologists have for many decades described singular immotile appendages known as primary cilia to be present on most cells in our bodies, cilial function(s) long remained an enigma. Driven largely by an ever increasing number of discoveries of genetic defects in primary cilia during the past decade, cilia were catapulted from a long lasting existence in obscurity into the bright spotlight in cell biology and medicine. The study by O’Toole et al. in this issue of the JCI adds a novel “enzymatic” facet to the rapidly growing information about these little cellular tails, by demonstrating that defects in the XPNPEP3 gene, which encodes mitochondrial and cytosolic splice variants of X-prolyl aminopeptidase 3, can cause nephronophthisis-like ciliopathy. Future studies are in order now to elucidate the cystogenic pathways affected by disrupted enzymatic function of XPNPEP3 in cilia-related cystogenic diseases.
Based on a flood of recent evidence, primary cilia are now heralded as sensory organelles for detection and transmission of a broad range of cues from the extracellular environment of cells (1), including mechanical and chemical information as diverse as fluid flow in kidneys, mechanical bone deformation, and light and odorant detection (2). By processing such physical and chemical information from the environment into molecular signals in development and postnatal growth and homeostasis, cilia can affect cell differentiation and polarity and cell cycle control (3).
Genetic damage to primary cilia results in a spectrum of perplexing disorders with seemingly disparate manifestations, now classified as ciliopathies. A growing list of bona fide ciliopathies at present includes Bardet-Biedl syndrome (BBS), nephronophthisis (NPHP), and Senior-Loken syndrome (SNLS), just to name a few. Common clinical features of ciliopathies include the hallmark renal cysts as well as liver disease, laterality defects, polydactyly, cognitive dysfunction, retinal degeneration, skeletal bone defects, and obesity among others (4).
Cilia are composed of a plasma membrane sheath, enveloping a microtubule-based axoneme that extends from the basal body. Cilia dismantle when cells enter cell cycle and reassemble during interphase. Growth and maintenance of cilia depend on microtubule-based transport motors, including kinesin II–dependent anterograde intraflagellar transport (IFT) and dynein-dependent retrograde IFT (Figure 1) (5). The cargo targeted to cilia by these transport processes includes, among others, components of several major signaling pathways, including sonic hedgehog receptors (6, 7) and WNT receptors (8). Thus, primary cilia modulate activities of major developmental signaling pathways involved in cell cycle control, differentiation, and planar cell polarity, and various ciliopathy-associated problems can be attributed to disrupted hedgehog and WNT signaling (2, 9, 10).
Ciliary and/or mitochondrial dysfunction as consequences of defective ciliary and mitochondrial XPNPEP3. Cilia consist of a microtubule-based axoneme enveloped by a specialized plasma membrane. The basal body is a microtubule-organizing center that anchors the axoneme. The transition zone (composed of transition fibers) filters molecules that enter or exit the cilium at the junction of the basal body. Axonemal and membrane components are transported in raft macromolecular particles (complexes A and B) by intraflagellar transport (IFT) along the axonemal doublet microtubules toward the tip complex, supported by microtubule end binding protein 1 (Eb1). Anterograde IFT toward the cilial tip is driven by heterotrimeric kinesin-2. Retrograde IFT back to the cell body occurs via the cytoplasmic motor protein dynein. As suggested in the study by O’Toole et al. in this issue of the JCI (13), a cytosolic 48-kDa form of XPNPEP3 may mediate enzymatic cleavage of known cystic-disease proteins ALMS1, LRRC50, and CEP290/NPHP6, and/or other yet unknown ciliary proteins, possibly regulating ciliary targeting or transport. O’Toole et al. report that loss of substrate cleavage, which is associated with defective XPNPEP3, leads to ciliary dysfunction. Similarly, loss of mitochondrial 51-kDa XPNPEP3 peptidase activity may result in failure to cleave yet unknown mitochondrial XPNPEP3 substrates and mitochondrial dysfunction. However, it is unclear at this time whether or how mitochondrial XPNPEP3 defects affect ciliary function. Image adapted with permission from Journal of the American Society of Nephrology (9).
Among the ciliopathies, NPHP is an autosomal recessive cystic kidney disease characterized by the triad of corticomedullary cysts, tubular basement membrane disruption, and tubulointerstitial nephropathy (9). Ten causative NPHP genes (NPHP1–NPHP9 and NPHP11) have been identified by positional cloning and a functional candidate gene approach, and their gene products, known as nephrocystins, localize to primary cilia (nephrocystins 1–5) and to basal bodies and centrosomes (nephrocystins 2–6, 8, and 9) (9, 11). An exception is NPHP7 (also known as GLI-similar protein 2 [GLIS2]), which is similar to the GLI family of transcription factors that are downstream targets of hedgehog signaling (12).
In a new and stunning twist on ciliopathies, in their new study in this issue of the JCI, O’Toole et al. report the presence of homozygous frameshift and splice-site mutations in the XPNPEP3 gene (which encodes X-prolyl aminopeptidase 3) in two families with an NPHP-like phenotype (13). Surprisingly, the XPNPEP3 protein has an N-terminal mitochondrial-targeting signal (MTS), and using recombinant expression in inner medullary collecting duct cells (IMCDs) of XPNPEP3-GFP chimeric proteins carrying the MTS, the authors confirmed the exclusive mitochondrial but not ciliary localization of the XPNPEP3 protein. While suppression of xpnpep3 in zebrafish phenocopied the developmental phenotypes observed in zebrafish ciliopathy morphants, the authors were surprised to find that expression of a cytosolic form of human XPNPEP3 lacking the MTS was able to rescue the cilia-related phenotype, indicating that mitochondrial localization of XPNPEP3 is not essential for its ciliary function.
XPNPEP3 belongs to the aminopeptidase P family of metallo-exopeptidases that specifically remove the N-terminal amino acid from peptides that have a proline residue in the second position after methionine (14). XPNPEP2 is a ubiquitous cell-surface membrane–bound peptidase that is thought to degrade peptides filtered by renal epithelium brush border membranes but may also be involved in bradykinin metabolism in endothelial cells (15). In contrast to XPNPEP2, physiological substrates or functions have not yet been identified for XPNPEP1 (which is a soluble cytosolic isoform) or XPNPEP3 (which is known to occur in two alternative splice forms) (Figure 2) (14). In contrast with the mitochondrial form of XPNPEP3, the cytosolic variant lacks the MTS (Figure 2). Importantly, both splice variants are expressed in kidney (14).
Two alternative splice forms of XPNPEP3 exist in the kidney. If exon 3 of XPNPEP3 is absent, the XPNPEP3 gene product starts with amino acid sequence MPWI and contains an N-terminal MTS that targets the protein to mitochondria. Exon 3 contains a stop codon (stp) in-frame, resulting in premature termination and removal of the MTS-containing gene product. The alternative XPNPEP3, lacking MTS, is translated from exon 4 AUG, possesses the starting amino acid sequence MSLI, and is likely localized to the cytosol. Mitochondrial XPNPEP3, i.e., the exon 3–spliced form, was used in the localization studies reported in this issue by O’Toole et al. (13).
How then may a poorly characterized enzyme with mitochondrial localization in distal tubules and intercalated collecting duct cells in human kidney cause cystic renal disease similar to NPHP, a bona fide ciliopathy? O’Toole et al. examined mitochondrial and respiratory chain functions in muscle biopsies and fibroblasts in affected individuals of the aforementioned kindreds (13). Mitochondriopathy with childhood end-stage renal disease and severe extrarenal manifestations (seizures, cardiomyopathy, and pancreatitis) was observed in two affected individuals in the Turkish kindred, carrying the homozygous frameshift mutation p.N311LfsX5. However, mitochondrial function was normal in affected adults with moderate renal disease from the Finnish kindred, carrying the less severe splice-site mutation p.G453C in XPNPEP3. These findings were inconsistent with the mitochondrial dysfunction hypothesis, and together with the observation that a cytosolic form of XPNPEP3 was able to rescue cilia-related phenotypes in the zebrafish studies, these data suggest that the functional defect underlying the NPHP-like renal phenotype might be independent of mitochondria.
The authors offer no explanation for the apparent contradiction between mitochondrial localization and cytosolic function of XPNPEP3 in NPHP-like phenotypes in their study but pursued another lead with acceptable results (13). They examined a pool of 426 likely ciliary protein sequences for candidate XPNPEP3 substrates and identified 51 putative candidates, including three proteins — centrosomal protein 290 kDa/NPHP6 (CEP290/NPHP6), Alstrom syndrome 1 (ALMS1), and leucine-rich repeat–containing 50 (LRRC50) — that are known to cause cystic disease (16–18). Indeed, synthetic peptides identical to the N-termini of all three substrate candidates were cleaved as predicted by the recombinant Escherichia coli ortholog of XPNPEP3, ecAPP. A key finding was the demonstration of the authors that an xpnpep3-mediated cleavage–resistant LRRC50 failed, while WT LRRC50 succeeded to rescue the cilia-related phenotype associated with endogenous lrrc50 suppression in zebrafish. The authors rightfully concluded that loss of activity of XPNPEP3-mediated enzymatic cleavage of substrates with ciliary and centrosomal functions may explain some forms of NPHP-like cystic renal disease, but their provocative speculation about an emerging link between mitochondria and ciliary dysfunction deserves further scrutiny.
Is it possible that the mitochondrial localization of XPNPEP3 shown in this report (13) is a red herring when it comes to ciliopathy pathways? The answer may well be affirmative. XPNPEP3 localization studies in the current report were performed exclusively using an XPNPEP3-GFP chimeric construct containing the MTS, which, not surprisingly, localized exclusively to mitochondria when expressed in murine IMCD3 cells. However, two alternative splice variants of XPNPEP3 were previously reported in kidney (14). The alternative splice variant studied by O’Toole et al. lacks exon 3 and initiates translation of a 507–amino acid XPNPEP3 isoform in exon 1, encoding an N-terminal MTS, which is removed by peptidases after import to mitochondria, resulting in an approximately 51-kDa mature mitochondrial enzyme (Figure 2). In contrast, exon 3 presents a stop codon in-frame to the exon 1 AUG, resulting in premature termination and removal of the truncated protein, and expression of a 428–amino acid isoform of XPNPEP3 devoid of MTS, translated from an AUG site located in exon 4 (14). Indeed, after probing for endogenous XPNPEP3 in IMCD3 cell lysates, the authors describe, in addition to the 51-kDa mitochondrial form, a second discrete band of XPNPEP3 of approximately 48 kDa, which can be predicted from the 428–amino acid cytosolic form of XPNPEP3 (13).
If the 48-kDa band is indeed the predicted cytosolic form of XPNPEP3, then the mitochondrial link may well be a red herring, because the NPHP-like disease observed in some individuals with XPNPEP3 mutations may be attributable to loss of proper cleavage of ciliary proteins by defective cytosolic XPNPEP3, as suggested by the overwhelming evidence from zebrafish studies (13). Of course, the same defect(s) in the mitochondrial form of XPNPEP3 may underlie some of the observed extrarenal manifestations, such as cardiomyopathy and seizures, which may be caused by mitochondrial dysfunction, as demonstrated in one kindred, and independent of ciliary dysfunction.
Perhaps the most intriguing prospect of the exciting study by O’Toole et al. (13) is that the novel discovery of functional mutations in the XPNPEP3 aminopeptidase in individuals presenting with NPHP-like ciliopathy may well lead to the further elucidation of two independent pathways associated with a distinct phenotypic spectrum: a cystogenic cilium-dependent pathway, dependent on defective cleavage of ciliary proteins by cytosolic XPNPEP3, and a mitochondriopathy, dependent on defective cleavage of mitochondrial substrates by mitochondrial XPNPEP3. Wow! Future work is needed to define the mitochondrial versus ciliary substrates and roles for hitherto rather obscure, spatially defined metallo-exopeptidases, encoded by a single novel human disease gene, XPNPEP3. Investigators concerned with ciliopathies and mitochondriopathies should stay tuned.
The author is supported by NIH grants 5R01DK056077, 5R01DK060043, 5R01DK073960, 3U01DK060995, and 1U01DK085688.
Conflict of interest: The author has declared that no conflict of interest exists.
Citation for this article: J Clin Invest. 2010;120(3):660–663. doi:10.1172/JCI42378