Molecular cloning and mapping of the human nicotinic acetylcholine receptor α10 (CHRNA10)

LR Lustig, H Peng, H Hiel, T Yamamoto, PA Fuchs - Genomics, 2001 - Elsevier
LR Lustig, H Peng, H Hiel, T Yamamoto, PA Fuchs
Genomics, 2001Elsevier
We report the isolation and initial characterization of a new member of the human nicotinic
acetylcholine receptor (nAChR) subunit family, α10 (CHRNA10), from both inner-ear
neuroepithelium and lymphoid tissue. The cDNA is 1959 nucleotides in length, with a coding
region predicting a protein of 451 amino acids that is 90% identical to rat α10. The α10 gene
was localized to chromosome 11p15. 5. Human α10 was detected in human inner-ear
tissue, tonsil, immortalized B-cells, cultured T-cells and peripheral blood lymphocytes using …
We report the isolation and initial characterization of a new member of the human nicotinic acetylcholine receptor (nAChR) subunit family, α10 (CHRNA10), from both inner-ear neuroepithelium and lymphoid tissue. The cDNA is 1959 nucleotides in length, with a coding region predicting a protein of 451 amino acids that is 90% identical to rat α10. The α10 gene was localized to chromosome 11p15.5. Human α10 was detected in human inner-ear tissue, tonsil, immortalized B-cells, cultured T-cells and peripheral blood lymphocytes using reverse transcriptase-polymerase chain reaction, Northern blot hybridization, and immunohistochemistry. We also detected the expression of the human nAChR α9 (CHRNA9) mRNA in these same tissues using RT-PCR and Northern blot hybridization.
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