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7/28/2019 Handigodu paper
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MMP13 F 56 S mutation is not associated with
Spondyloepimetaphyseal Dysplasia:Handigodu type
Pulamaghatta N. Venugopal1, Cholendra Arja
2, Adimoolam Chandrasekar
1,
Arjun Rao1
1Anthropological Survey of India, Southern Regional Centre, Bogadi, Mysore,
Karnataka, 570026, India; E-mail: [email protected] of Human Genetics, Department of Anthropology, Sri Venkateshwara
University, Tirupati, Andhra Pradesh, 517502, India
ABSTRACT
Handigodu (HG) syndrome is a disorder of the osteoarticular system prevalent in few villages of two districts
of the Karnataka state in Southern India. The condition was first observed from a Handigodu village, hence itsname. Subsequent multidisciplinary study by the Indian Council of Medical Research (ICMR), Government of
India revealed that Handigodu syndrome could be considered as late onset spondylo epi (meta) physeal
dysplasia. Genomic DNA was isolated from 5ml of peripherial blood samples of Handigodu syndrome
affected individuals and controls further it has been sequenced exon 2 of MMP 13 gene to identify the
mutation at the codon F 56 S. The sequence analysis of exon 2 of MMP13 did not reveal any polymorphisms,
including the functional F 56 S, in both patients and controls. MMP 13 is important for the replacement of
cartilage with bone and not in the elongation of long bones, which may be controlled by its upstream
signalling molecules. This explains the absence of MMP 13 mutation in HG syndrome patients and suggests a
possibility of defect in the upstream signalling molecules.
Keywords: Handigodu Syndrome, Spondyloepimetaphyseal Dysplasia, MMP13, endochondral ossification
INTRODUCTION
Handigodu (HG) syndrome is a rare and painful osteoarthritic disorder endemic to the Malnadregion (Shimoga and Chikkamaglur districts) of Karnataka state, India. The first case of the disease
was reported from Handigodu Village of Sagar Taluk of Shimoga District, hence the name of thedisease. Despite several studies the condition continues to remain a major medical problem of these
socially deprived people. The affected individuals are categorized into 3 phenotypes: type I
(predominantly hip-joint pains), type II (predominantly dysplastic), and type III (dwarf). Dysplasiaof hip joints and spine is often associated with osteoarthritis. Radiological findings in HG syndrome
(Figure 1) include narrowing of the joint space, irregularity and sclerosis of articular margins,
presence of osteophytes, protrusio acetabuli, flattening of femoral head, flattening andfragmentation of epiphyses, coxa vara, subchondral sclerosis, small pelvis, broad short neck,
wedge-shaped vertebrae, irregularity of end plates, and platyspondyly [1].Since its discovery in 1975, the etiology of this disease remains unknown till day. Earlier
studies conducted by Indian Council of Medical Research and National Institute of Nutrition could
not attribute the cause to any ecological disturbances, like trace metal toxicities or undue exposureto pesticides. An earlier study identified this disease as a type of spondyloepimetaphyseal dysplasia
(SEMD) which follows a predominantly autosomal dominant pattern of inheritance [1]. However,
its pattern of inheritance is not validated [2,3]. The earlier study [4] mapped the locus, which is
Research Article, Biotechnol. Bioinf. Bioeng. 2011, 1(2):269-273© 2011 Society for Applied Biotechnology. Printed in India.
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responsible for SEMD Missouri type (SEMDMO) on chromosome 11 (11q14.3-23.2). Further, the
sequence analysis in this region identified a mutation in the exon 2 (F 56 S) in the MMP13 gene,which leads to intracellular autoactivation and degradation of the mutant proenzyme, which is likely
to be misfolded, with the resulting MMP13 deficiency causing SEMD MO [4]. As radiologicalfeatures of SEMDMO are similar to SEMDHG, we tested HG syndrome patients for F 56 S mutation
in exon2 of MMP13.
Figure 1. Radiographic abnormalities of SEMDHG.
MATERIALS AND METHODS
All patients included in the study were those identified by Indian Council of Medical Research on
the basis of radiological findings. Information regarding patients was obtained from the Medical
officer of HG Syndrome Mobile Health Unit of Shimoga District. About 5ml of peripheral blood
was collected from 200 SEMDHG patients and 100 controls after receiving their informed consent.Genomic DNA was isolated using phenol-chloroform method. Amplification of exon 2 of MMP13
was carried out in a 10µl reaction mixture using the forward primer 5'-TGCCAATCCTGATGATG
CGGT-3' and reverse primer 5'-GTGGAACTCTTCATCTTGAGCACT-3'. The reactions were
performed with an initial denaturing cycle of 5 minutes at 95C, followed by 35 cycles at 94C for
1minute, 63.8C for 45 second, 72C for 2 minutes 30 second, and a final extension for 7 minutes at
72C. The polymerase chain reaction product was confirmed on a 2% w/v agarose gel. Polymerasechain reaction products were sequenced using Applied Bio systems ABI 3730 sequencer.
RESULTS AND DISCUSSION
The sequence analysis of exon 2 of MMP13 did not reveal any polymorphisms, including thefunctional F 56 S, in both patients and controls (Figure 2). Fetal bone development is a complex
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process, which occurs by means of intramembranous ossification and endochondral ossification.
The relevance of MMP13 in SEMDHG comes from its indispensable role in endochondralossification in which long bone-like limbs are formed from cartilage. Periarticular chondrocytes first
proliferate and differentiate into columnar chondrocytes. Columnar chondrocytes determine thelength of the bone. The columnar chondrocytes proliferate and differentiate into prehypertrophic
chondrocytes, which in turn differentiate into hypertrophic chondrocytes.
Figure 2. Electrophorograph of the position of 56 codon.
Growth plate lies between the two centres of ossification. Formation of bone proceeds toward
the plate from both the directions, but the growth of cartilage is faster on one side (diaphysis) whichallows for elongation. During endochondral ossification, the mitotically active proliferatingchondrocytes produce an extracellular matrix composed principally of collagen type II. As
chondrocytes differentiate (postmitotic), they synthesize collagen X [5]. The most mature
hypertrophic chondrocytes produce alkaline phosphatase which deposits calcium in thecartilaginous matrix. The hypertrophic chondrocytes undergo apoptosis as nutrients can no longer
diffuse through the calcified matrix. This creates cavities in the bone. The hypertrophicchondrocytes also express vascular endothelial growth factor, which allows the corresponding area
to be invaded by blood vessels which brings into the cavity hemotopoietic cells, osteoclast, and
osteoblasts. The osteoblasts then produce osteoid, which are a protein mixture chiefly, composed of type I collagen.
The length of the columnar region is determined by the rate of differentiation of periarticular
into columnar chondrocytes, the rate of proliferation of columnar cells, and the rate of
differentiation of columnar to hypertrophic chondrocytes. Hypertrophic chondrocytes express Indian hedgehog (IHH) [6] which is a member of hedgehog family of secreted signaling molecules[7]. Parathyroid hormone-related peptide (PTHrP) is expressed by periarticular chondrocytes [5].
PTHrP and IHH are important regulators of cartilage development [8]. IHH, produced by
prehypertrophic and hypertrophic chondrocytes, stimulates production of PTHrP by periarticular chondrocytes [9,10]. IHH directly acts on periarticular chondrocytes to stimulate their
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differentiation to columnar chondrocytes and also stimulates the synthesis of PTHrP by periarticular
chondrocytes [8]. PTHrP, thereafter, binds to its receptor PTH/PTHrP receptor 1 (PTHR1), which isexpressed at low levels by proliferating chondrocytes in columns and at higher levels by
prehypertrophic chondrocytes [11] and prevents premature differentiation of chondrocytes intohypertrophic chondrocytes and thereby suppresses premature expression of IHH [8]. This negative
feed-back loop exerted by IHH on PTHrP controls the synchrony of chondrocyte differentiation and
regulates columnar chondrocyte mass [8,12,13].The PTHrP also signals (through its receptor PTHR1) the core binding factor-α-1 which
initiates the transcription of their downstream target MMP 13 [14-16]. The MMP 13 is strongly
induced in hypertrophic chondrocytes, periosteal cells, and osteoblasts during endochondralossification and intramembranous ossification [17-22]. It can degrade collagen types I, II, III and X
[22,23]. The cartilage matrix composed of types II and X collagen is degraded and eventuallycalcified. This loss of collagen at the hypertrophic zone in the growth plate is associated with
increased MMP 13 activity. MMP13 deficiency, therefore, would prevent orderly ECM degradation
in developing growth plates with accumulation of types II and X collagens, and disturbendochondral ossification [4].
Even if MMP 13 is important for the replacement of cartilage with bone and not in theelongation of long bones, which may be controlled by its upstream signalling molecules. This
explains the absence of MMP 13 mutation in HG syndrome patients and suggests a possibility of defect in the upstream signalling molecules. Although genome-wide linkage study is the ultimate
tool when it comes to mapping disease loci, availability of families with multiple affected members
is a severe limitation. Meanwhile in a disease like SEMDHG with complex etiology, genes that could
be postulated to be functionally related to the disease can be tested directly for their involvement inthe disease process. Recent study [24] involving HG patients have identified defective
hydroxylation of proline residues in patients and a possibility of defective vitamin D receptor [25].Future studies are warranted to focus on the polymorphisms of the genes in concern.
Acknowledgments: The authors wish to acknowledge Ministry of Culture, Government of India for
permitting to carry out this project under the national project, ‘DNA Polymorphism and Diseases’.We thank the social workers, Mr. Chandrashekar Bhat, Mrs. Rajakka and Dr. Najunda DC, Deputy
Director cum Reader, CFSEIP, University of Mysore, Mysore in mobilizing the patients and their
families. Authors are also thankful to Directorate of Health and Family Welfare Services,Government of Karnataka for providing their logistic support to this study. Above all, authors
express their gratitude to the subjects who have willingly participated in providing blood samples.
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