Bajaj, Vineeta and Markandaya, Manjunath and Krishna, Lingegowda and Kumar, Arun (2004) Paternal imprinting of the SLC22A1LS gene located in the human chromosome segment 11p15.5. In: BMC Genetics, 5 (13). pp. 1-4.
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Abstract
Background: Genomic imprinting is an epigenetic chromosomal modification in the gametes or zygotes that results in a non-random monoallelic expression of specific autosomal genes depending upon their parent of origin. Approximately 44 human genes have been reported to be imprinted. A majority of them are clustered, including some on chromosome segment 11p15.5. We report here the imprinting status of the SLC22A1LS gene from the human chromosome segment 11p15.5 Results: In order to test for allele specific expression patterns, PCR primer sets from the SLC22A1LS gene were used to look for heterozygosity in DNA samples from 17 spontaneous abortuses using PCR-SSCP and DNA sequence analyses. cDNA samples from different tissues of spontaneous abortuses showing heterozygosity were subjected to PCR-SSCP analysis to determine the allele specific expression pattern. PCR-SSCP analysis revealed heterozygosity in two of the 17 abortuses examined. DNA sequence analysis showed that the heterozygosity is caused by a G>A change at nucleotide position 473 (c.473G>A) in exon 4 of the SLC22A1LS gene. PCR-SSCP analysis suggested that this gene is paternally imprinted in five fetal tissues examined. Conclusions: This study reports the imprinting status of the SLC22A1LS gene for the first time. The results suggest imprinting of the paternal allele of this gene in five fetal tissues: brain, liver, placenta, kidneys and lungs.
Item Type: | Journal Article |
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Publication: | BMC Genetics |
Publisher: | BioMed Central |
Additional Information: | The copyright belongs to BioMed Central |
Department/Centre: | Division of Biological Sciences > Molecular Reproduction, Development & Genetics |
Date Deposited: | 25 Nov 2004 |
Last Modified: | 19 Sep 2010 04:17 |
URI: | http://eprints.iisc.ac.in/id/eprint/2362 |
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