alexa Pleiotropy of Presenilins | Open Access Journals
ISSN: 2161-1041
Hereditary Genetics: Current Research
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Pleiotropy of Presenilins

Airong Li* and Rudolph E Tanzi

Genetics and Aging Research Unit, Department of Neurology, Mass General Institute for Neurodegenerative Diseases, Massachusetts General Hospital and Harvard Medical School, MA, USA

*Corresponding Author:
Airong Li
Genetics and Aging Research Unit
Massachusetts General Hospital, Harvard Medical School
CNY114, 16th Street Charlestown, MA 02129, USA
Tel: 617-724-9397
Fax: 617-724-1823
E-mail:[email protected]

Received Date: October 18, 2012; Accepted Date: October 18, 2012; Published Date: October 20, 2012

Citation: Li A, Tanzi RE (2012) Pleiotropy of Presenilins. Hereditary Genet 2: e105. doi: 10.4172/2161-1041.1000e105

Copyright: © 2012 Li A, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

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Abstract

Pleiotropy genes affect multiple and apparently unrelated phenotypes. Here we describe pleiotropy gene
presenilins, mutations in which have been detected in three genetically heterogeneous diseases: early-onset familial Alzheimer’s disease, familial or sporadic dilated cardiomyopathy, and familial hidradenitis suppurativa.

Pleiotropy describes the genetic effect of a single gene on multiple phenotypic traits, or genetic variations in a single gene lead to multiple unrelated traits or diseases [1]. In contrast to pleiotropy, genetic heterogeneity means that a single phenotype or genetic disorder may be caused by different alleles in the same gene (allelic heterogeneity), or variations in two or more unrelated gene loci (locus heterogeneity) [2]. Pleiotropy genes affect multiple and apparently unrelated phenotypes [3], such as mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene led to either cystic fibrosis [4] or congenital bilateral absence of vas deferens [5]; mutations in the phenylalanine hydroxylase (PAH) gene caused not only phenylketonuria (PKU) but also a number of phenotypes, including mental retardation, eczema, and pigment defects [6]. The underlying mechanism of pleiotropy genes may include that their encoded gene products either are used by various cells or have different functional targets. For example, loss-of-function mutations in the RET protooncogene (RET) gene led to Hirschsprung disease (HSCR) by impairing its tyrosine kinase activity (i.e. R972G), disrupting the correct maturation of the RET protein and its transport to the cell surface (i.e. S32L and F393L) [7,8], or loss of function effect in homozygous condition (i.e. C620R/C620R) [9]. In contrast, two gain-of-function mutations in the RET, heterozygous C620R resulting in a dominant gain of function effect with low penetrance [9], and the Y606C increasing receptor dimerization and constitutively activating receptor, were associated with multiple endocrine neoplasia type 2A (MEN2A) [9-11].

Presenilins were first identified in screens for mutations causing early onset forms of familial Alzheimer’s disease (AD) in 1995 [12-14]. Of two presenilin genes in human, PSEN1 is located on chromosome 14 that encodes presenilin 1 (PS1), and PSEN2 is on chromosome 1 that codes for presenilin 2 (PS2). PS1 and PS2 are highly conserved polytopic membrane proteins that form the catalytic centre of the γ-secretase complex [15]. The γ-secretase consists of a large protein complex that include at least four proteins, presenilins (PS1, PS2), nicastrin (NCSTN), anterior pharynx defective 1 (APH1) and presenilin enhancer 2 (PEN2), and is responsible for the proteolytic processing of a variety of membrane-associated fragments derived from type I integral membrane proteins, including the amyloid precursor protein (APP) and the Notch [16]. Notch receptor cleavage within the plasma membrane by γ-secretase results in the release and translocation of the Notch intracellular domain (NICD) into the nucleus to execute Notch signaling, which is critical for development. Presenilin mutations have been detected in three unrelated and genetically heterogeneous diseases: early-onset familial AD [15], familial or sporadic dilated cardiomyopathy (DCM) [17,18], and familial hidradenitis suppurativa (HS) [19].

Presenilin and AD

AD is a progressive neurodegenerative disease and the most common form of dementia in the elderly, affecting one in 10 individuals over 65 and nearly half over 85 years old (http://www.alz.org/) [20]. AD is characterized clinically by cognitive decline accompanied by neuronal loss and the formation of neurofibrillary tangles (NFTs) and insoluble toxic amyloid plaques in the brain [21]. Genetically, AD is heterogeneous and complex [22]. The majority of AD patients have the late-onset form (>60 years). Roughly 5-10% AD occurs in families where the disease is autosomal dominantly inherited with full penetrance and early onset (<60 years). Presenilin mutations underlie the majority of cases of early-onset familial AD [15]. To date, approximately 167 mutations in PSEN1 and 14 mutations in PSEN2 have been identified in familial AD patients (http://www. alz.org/; http://www.molgen.ua.ac.be/ADMutations). Majority of mutations in PSEN1 and PSEN2 are missense mutations that result in single amino-acid substitutions, and other type of mutations such as in-frame deletions, insertions or splice site mutations are also found (http://www.molgen.ua.ac.be/ADMutations). PSEN2-K115E fx10 was the only frame-shift mutation detected in presenilin coding region in AD patients [23].

Mutations in presenilins alter the proteolytic processing of APP by aberrant γ-secretase activities that results in increased neurotoxic β-amyloid (Aβ) 42 production [21]. Moreover, PSEN1 mutations may perturb cellular Ca2+ homeostasis thereby render neurons more vulnerable to excitotoxity and apoptosis to promote neuronal degeneration [24-27]. Transgenic mice overexpressing the early onset familial AD-associated APP and PSEN1 mutations resulted in accelerated Aβ accumulation and associative learning deficits [28]. A transgenic conditional double knockout mouse lacking both PSEN1 and PSEN2 in the postnatal forebrain showed impaired hippocampal memory and synaptic plasticity and developed neurodegeneration of the cerebral cortex [29]. These findings indicate that loss of function in presenilins plays an important role in AD pathogenesis.

Presenilin and DCM

DCM is defined clinically by dilation and impaired contraction of one or both ventricles. DCM occurs in all ages, most common between 20-60 years. DCM causes roughly one-third of cases of congestive heart failure [30]. About 20-40% of patients have familial forms of the disease [31]. Genetically, DCM is heterogeneous [32,33]. Mutations in presenilins have been detected in all clinically affected subjects with heart failure from three DCM families [17], as well as four severe sporadic DCM patients who were performed heart transplantation due to heart failure [18].

So far six promoter region variants or missense mutations in presenilins have been identified in patients with DCM [17,18]. Two PSEN1 5’ promoter region variants, -92delC and -21G>A, led to a significant reduction in transcriptional activities and a decreased expression of PS1 protein in the myocardium, suggesting loss of function [18]. Two PSEN1 missense mutations, PSEN1-E318G and PSEN1-D333G, were 15 amino acids apart and located in a “hot spot” exclusively in a large hydrophilic cytoplasmic loop between PS1 transmembrane domains six and seven. This region contained critical functional domains which were processed by endoproteolysis [34], and were essential for the interaction between PS1 and other proteins [35], such as binding PS1 to ubiquilin1, which was associated with an increased susceptibility risk for late-onset AD [35,36]. High prevalence of PSEN1 missense mutations also occurred in or around in this loop region in familial AD [37-39], consisting of 12.6% (21/167) of all reported PSEN1 mutations (http://www.hgmd.cf.ac.uk/). Two PSEN2 missense mutations, PSEN2-R62H and PSEN2-S130L, were located in a “hot spot” of the PS2 NH2 terminus [17,18]. Calcium signaling was altered in cultured skin fibroblasts from PSEN1-D333G and PSEN2- S130L mutation carriers [17]. The PSEN2-R62H missense mutation enhanced PS2 degradation, reduced PS2 stability in mouse embryonic fibroblasts, and altered compromised PS2 function in Notch signaling in C. elegans [40]. Interestingly, these two “hot spots” in which missense mutations in presenilins were clustered are highly divergent regions of PS1 and PS2, as both proteins share extensive sequence identity along their entire lengths except their NH2-terminus and the second half of their hydrophilic loop regions. Presenilin missense mutations in divergent regions may pay an important role in DCM pathogenesis by modulating different functions of PS1 and PS2 [18].

PSEN1 and PSEN2 were strongly expressed in the heart and essential for cardiac morphogenesis [41,42]. Mice null for PS1 were either dead at birth (Ps1-/-) or embryonically lethal (Ps1-/-/Ps2-/+), exhibiting multiple developmental defects including a cardiac anomaly [42]. Studies in transgenic Drosophila models with an emerging optical coherence tomography imaging technology demonstrated that changes in presenilin level either by overexpression or silencing of the Drosophila ortholog of presenilins led to cardiac dysfunction in adult flies, owing to aberrant calcium channel receptor activities and disrupted Wnt signaling transduction, indicating a pathogenic role for presenilin mutations in DCM pathogenesis [43].

Presenilin and HS

HS is a chronic inflammatory skin disease and severe form of acne (acne inversa). HS affects the apocrine sweat glands or sebaceous glands most commonly in areas of the underarms, breasts, inner thighs, groin and buttocks, and often results in chronically draining sinus tracks, wounds, scarred and tissue immobility [44]. The prevalence of HS is approximately 1 in 300 persons, with females affected three times more often than males. Genetics plays a significant role in the etiology of HS. Genetically, HS is heterogeneous [45].

A single PSEN1-P242LfsX11 frame-shift mutation was found to segregate with HS in a family with HS where the disease was autosomal dominantly inherited [19]. In addition, heterozygous loss-of-function mutations were found in genes encoding the other components and cofactor of γ-secretase complex: including NCSTN (R117X, E584DfsX44, and A486_T517del) and PEN2 (F23LfsX46 and F94SfsX49) in patients with familial HS [19]. RT-PCR showed a significantly reduced PSEN1 or NCSTN transcript expression in peripheral lymphocytes of the affected individuals carrying a PSEN1 or NCSTN mutation. These findings suggest that loss of function in the γ-secretase component genes may be a genetic basis for familial HS [19]. None of 15 HS patients from HS families at 50 years or older carrying a mutation in a γ-secretase complex component had symptoms of AD [19]. Notably, HS-associated PSEN1-P242LfsX11 [19] and AD-associated PSEN2-K115E fx10 [23] were only frameshift mutations detected in presenilin coding regions that resulted in premature termination codons.

Collectively, mutations or variants in presenilins were detected in patients with AD, DCM or HS, which indicate pleiotropy of presenilins. Functional analyses have suggested that the mutations or variants in presenilins contribute to AD, DCM or HS pathogenesis through loss of gene function. Further studies are warranted to elucidate the molecular mechanisms involved in how mutations or variants in the same presenilin may result in distinct pathogenic features in three unrelated diseases: neurodegeneration in AD, cardiomyopathy in DCM, or acne in HS.

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