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Volume 58, Issue 1, Pages 16-22 (1 July 2005)


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MLC1 Gene Is Associated with Schizophrenia and Bipolar Disorder in Southern India

Ranjana Vermaaemail address, Mitali Mukerjia, Deepak Grovera, Chandrika B-Raoa, Swapan Kumar Dasa, Shobana Kubendranb, Sanjeev Jainb, Samir K. BrahmachariaCorresponding Author Informationemail address

Received 10 November 2004; received in revised form 2 March 2005; accepted 16 March 2005. published online 09 May 2005.

Background

Chromosome 22q13 has shown linkage with schizophrenia (SCZ) and bipolar affective disorder (BPAD). A missense mutation in MLC1 (putative cation-channel gene on 22q13) co-segregating with periodic catatonic schizophrenia has been reported. We have investigated the relationship of MLC1 with SCZ and BPAD in Southern India.

Methods

All exons and flanking intronic sequences of MLC1 were screened for novel variations. Case-control (216 BPAD, 193 SCZ, 116 control subjects) and family-based analyses (113 BPAD, 107 SCZ families) were performed to evaluate association of MLC1 with these disorders.

Results

We found 33 MLC1 sequence variations, including three novel mutations: Val210Ile, Leu308Gln, and Arg328His in six BPAD cases and Val210Ile in one control individual. Minor allele of a common variation, ss16339182 (in ∼6 Kb Linkage-Disequilibrium [LD]-block) was associated with BPAD in case-control (p = .03) and family-based analyses (transmitted/nontransmitted [T/NT]-44/20; p = .003). Association was observed for rs2235349 and rs2076137 with SCZ and ss16339163 with BPAD in case-control study. Using Block 2 haplotype tagging single nucleotide polymorphisms (htSNPs), GC haplotype revealed association (p = .02) and excess transmission (p = .002) with BPAD.

Conclusions

Association of MLC1 with SCZ and BPAD suggests involvement of a common pathway. Rare missense mutations and common variants associated with BPAD favors hypothesis about likely involvement of both rare and common polymorphisms in etiology of this complex disorder.

a Functional Genomics Unit, Institute of Genomics and Integrative Biology (CSIR), Delhi, India

b Molecular Genetics Laboratory, Department of Psychiatry, National Institute of Mental Health and Neurosciences, Bangalore, India.

Corresponding Author InformationAddress reprint requests to Dr. Samir K. Brahmachari, Functional Genomics Unit, Institute of Genomics and Integrative Biology (CSIR), Delhi University Campus, Mall Road, Delhi-110007, India

PII: S0006-3223(05)00370-7

doi:10.1016/j.biopsych.2005.03.027


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