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Editorials |
Department of Pediatrics, University of Southern California Keck School of Medicine, Los Angeles, CA
Correspondence: Dr. Kevin V. Lemley, Division of Nephrology, MS #40, Childrens Hospital Los Angeles, 4650 Sunset Boulevard, Los Angeles, CA 90027. Phone: 323-361-2102; Fax: 323-361-1184; E-mail: klemley{at}chla.usc.edu
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The discovery of mutations in these same genes outside the clinical phenotypes of SRNS in which they were first described has shed new light on the complexity of the genetic basis of SRNS. Mutations in NPHS2 have been found in a large number of infants with CNS (more commonly than NPHS1 mutations in one study3). Genetic heterogeneity of CNS, including triallelic involvement of NPHS1 and NPHS2, has also been described.4 Even within the classical age range of SRNS caused by NPHS2 mutations, nonsense or homozygous p.R138Q mutations have been shown to present earlier than (other) missense mutations.5 Now Philippe et al.6 report in this issue of JASN that mutations in NPHS1 are found in some patients with SRNS presenting outside the neonatal period. As with neonatal presentation of triallelic NPHS1/NPHS2 mutations,4 these individuals manifest histologic patterns quite different from classical CNS.
Why are these mutations now being found outside their original phenotypes? In part, this may be because genotyping of such cases has so far been difficult and expensive, so mutations in a particular gene have generally not been sought in patients "outside" the classical phenotype. Could these extended phenotypes also be due to novel mutations? At least one mutation in NPHS2 (leading to p.R138Q in podocin) has been described both in CNS3,4 and in infantile and childhood-onset SRNS.2,4 This is also the case for at least two of the 14 mutations in NPHS1 reported by Philippe et al.,6 which have been reported before in the context of classical CNS, in one case (p.R460Q) associated as a heterozygous mutation with neonatal onset of nephrotic syndrome leading to kidney failure at 10 mo of age.7 Alternatively, does SRNS appear later in some patients because they are compound heterozygotes with one "mild" mutation in NPHS1? Philippe et al. present in vitro functional evidence for normal trafficking to the plasma membrane and protein–protein interactions of nephrin in most of their missense mutations. At the same time, two of the mutations with some preserved in vitro functions were severe enough to lead to kidney failure by 13 yr of age.
Because Philippe et al. excluded in advance patients having detectable NPHS2 or WT1 mutations, the interesting question of oligogenic involvement of mutations in NPHS1 and in one or both of these other genes cannot be addressed from their study. A recent report8 suggested that bigenic (digenic) mutations in five genes (WT1, NPHS1, NPHS2, CD2AP, and PLCE1) may account for a substantial number (four of 19) of cases of sporadic childhood-onset SRNS, so undetected digenic mutations could conceivably explain nonclassical phenotypes associated with NPHS1 mutations. The occurrence of heterozygous NPHS1 mutations3,9 suggests that digenic mutations also may occur in classical presentations of CNS. Clearly, we do not as yet understand the genetic basis for phenotypic variation in SRNS; simple monogenic models are certainly inadequate.
A complex form of inheritance has been well described in other genetic diseases affecting the kidney. Bardet-Biedl syndrome (BBS) is associated with mutations in 12 different genes and shows broad phenotypic variability.10 Katsanis11 proposed that this variability is in part due to an oligogenic (triallelic) mode of inheritance, based on epistatic interactions of heterozygous (missense) mutations in a BBS-associated gene with homozygous or compound heterozygous mutations in another BBS-associated gene. Mutations in these genes presumably interact because the genes underlie a system (or module12) of interacting proteins (in this case, proteins of the sensory cilia and central body in tubule cells). Similarly, because a large number of genes are involved in the nephronophthisis (NPHP) spectrum, Hildebrandt and colleagues13 investigated and detected cases of oligogenic inheritance in their NPHP patient population. As with BBS, nephronophthisis is characterized by broad phenotypic variation. The protein products of the NPHP-associated genes also interact in the primary cilia of renal tubules.
Given the aforementioned examples of BBS and NPHP, it should hardly be surprising if digenic mechanisms were also operative in at least some cases of SRNS. Podocyte function depends on the integrated structural and signaling roles of a large number of interacting foot process proteins, ranging from nephrin and Neph1 at the slit diaphragm, to scaffolding proteins such as CD2AP and ZO-1, to the actin cytoskeleton and its "bundling" protein, 
-actinin-4. In aggregate, heterozygous epistatic modifying gene mutations may not be particularly rare. NPHS1 heterozygotes alone may have a frequency approaching 1% in many populations, and there may be dozens of genes (e.g., FAT1, FAT2, Neph1, Neph2, P-cadherin, CASK), mutations of which could have epistatic interactions with "classical" homozygous or compound heterozygous mutations in genes previously recognized as associated with SRNS. Clinical phenotypes are being increasingly appreciated for heterozygous mutations in genes originally implicated in classic Mendelian recessive diseases.14 In well-mixed communities, it is possible that digenic or triallelic combinations of heterozygous mutations of interacting genes are more common than classical "pure" autosomal recessive cases in SRNS, albeit perhaps more subtle in their presentation.
The findings of Hinkes et al.3 and Philippe et al.6 and their colleagues highlight some of the limitations of the purely descriptive, clinicopathologic diagnoses of SRNS that we use today. We still lack a robust molecular diagnostic framework for many cases of SRNS. Integration of patient genotype for multiple podocyte-expressed genes and biopsy gene expression15 together with novel histologic descriptions based on podocyte number or patterns of expression of specific podocyte proteins may allow us to parse complex genetic forms of SRNS into a limited number of disease-related modules that better reflect physiologically linked intracellular systems of podocyte proteins. The complexity of the genetics may seem daunting, but the opportunity to forge new pathogenetic and diagnostic insights may be worth the effort.
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See related article, "Nephrin Mutations Can Cause Childhood-Onset Steroid-Resistant Nephrotic Syndrome," on pages 1871–1878.
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