MMP13 F 56 S mutation is not associated with Spondyloepimetaphyseal Dysplasia:Handigodu type

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 its name. 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.

Updating Phylogeny of Mitochondrial DNA Macrohaplogroup M in India: Dispersal of Modern Human in South Asian Corridor

To construct maternal phylogeny and prehistoric dispersals of modern human being in the Indian sub continent, a diverse subset of 641 complete mitochondrial DNA (mtDNA) genomes belonging to macrohaplogroup M was chosen from a total collection of 2,783 control-region sequences, sampled from 26 selected tribal populations of India. On the basis of complete mtDNA sequencing, we identified 12 new haplogroups - M53 to M64; redefined/ascertained and characterized haplogroups M2, M3, M4, M5, M6, M89C9Z, M9, M10, M11, M12-G, D, M18, M30, M33, M35, M37, M38, M39, M40, M41, M43, M45 and M49, which were previously described by control and/or coding-region polymorphisms. Our results indicate that the mtDNA
lineages reported in the present study (except East Asian lineages M89C9Z, M9, M10, M11, M12-G, D ) are restricted to Indian region.The deep rooted lineages of macrohaplogroup ‘M’ suggest in-situ origin of these haplogroups in India. Most of these deep rooting lineages are represented by multiple ethnic/linguist groups of India. Hierarchical analysis of molecular variation (AMOVA) shows substantial subdivisions among the tribes of India (FST = 0.16164). The current Indian mtDNA gene pool was shaped by the initial settlers and was galvanized by minor events of gene flow from the east and west to the restricted zones. Northeast Indian mtDNA pool harbors region specific lineages, other Indian lineages and East Asian lineages. We also suggest the establishment of an East Asian gene in North East India through admixture rather than replacement.
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Detailed mtDNA genotypes permit a reassessment of the settlement and population structure of the Andaman Islands

The population genetics of the Indian subcontinent is central to understanding early human prehistory due to its strategic location on the proposed corridor of human movement from Africa to Australia during the late Pleistocene. Previous genetic research using mtDNA has emphasized the relative isolation of the late Pleistocene colonizers, and the physically isolated Andaman Island populations of Island South-East Asia remain the source of claims supporting an early split between the populations that formed the patchy settlement pattern along the coast of the Indian Ocean. Using whole-genome sequencing, combined with multiplexed SNP typing, this study investigates the deep structure of mtDNA haplogroups M31 and M32 in India and the Andaman Islands. The identification of a so far unnoticed rare polymorphism shared between these two lineages suggests that they are actually sister groups within a single haplogroup, M3132. The enhanced resolution of M31 allows for the inference of a more recent colonization of the Andaman Islands than previously suggested, but cannot reject the very early peopling scenario. We further demonstrate a widespread overlap of mtDNA and cultural markers between the two major language groups of the Andaman archipelago. Given the completeness of the genealogy based on whole genome sequences, and the multiple scenarios for the peopling of the Andaman Islands sustained by this inferred genealogy, our study hints that further mtDNA based phylogeographic studies are unlikely to unequivocally support any one of these possibilities. Am J Phys Anthropol, 2008

Influence of educational levels of the spouses on consanguinity among three endogamous groups of Andhra Pradesh, South India

The highest values of consanguinity was found among “Kamma” (45.0%), “Ediga” (47.5%) and “Mala” (55.7%) who occupy different strata of Indian caste hierarchy. In the way of searchout the factors influencing consanguineous marriages, the present paper finda the negative relationship between educational levels of the spouses and consanguinity. The educational levels of men has significant effect on the frequency of consanguinious marriages among “Kamma” and “Mala”. However, further analysis deplore significant differences in the mean levels consanguinity between educational groups. It divulge low level of higher education among the populations. Only 12% of men and 1.6% of women have degree level and above education in the total sample.

Chandrasekar, A. 1995. Influence of educational levels of the spouses on consanguinity among three endogamous groups of Andhra Pradesh, South India. International Journal of Anthropology 10 (2-3):125-132.
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YAP insertion signature in South Asia

Reports, for the first time, high frequencies (8-65%) of Y Alu polymorphic (YAP) insertion in northeast Indian tribes. All seven Jarawa samples from the Andaman and Nicobar islands had the YAP insertion, in conformity with an earlier study of Andaman Islanders. One isolated case with haplotype E* was found in Dungri Bhill, a western Indian population, while YAP insertion in northeast India and Andaman tribes was found in association with haplotype D* (M168, M174). YAP insertion frequencies reported in the mainland Indian populations are negligible, according to previous studies. Genetic drift may be the causative factor for the variable frequency of the YAP insertion in the mainland populations, while the founder effect may have resulted in the highest incidence of haplotype D among the Andaman Islanders. The results of YAP insertion and the evidence of previous mtDNA studies indicate an early out of Africa migration to the Andaman and Nicobar Islands. The findings of YAP insertion in northeast Indian tribes are very significant for understanding the evolutionary history of the region.
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