TY - JOUR
T1 - Homologous loci DXYS156X and DXYS156Y contain a polymorphic pentanucleotide repeat (TAAAA)n and map to human X and Y chromosomes
AU - Chen, Haiming
AU - Lowther, William
AU - Avramopoulos, Dimitrios
AU - Antonarakis, Stylianos E.
PY - 1994
Y1 - 1994
N2 - We report the isolation and characterization of a polymorphic pentanucleotide repeat (TAAAA)n, which was mapped to human chromosomes X and Y (loci DXYS156X and DXYS156Y) by PCR amplification of DNA from a monochromosomal somatic cell hybrid panel (NIGMS panel 2). The (TAAAA)n repeat of loci DXYS156 occurs within a human LINE element at a position where the consensus sequence contains a single TAAAA motif. In 72 unrelated CEPH individuals seven alleles were detected which ranged in size from 125 to 165 bp in 5 bp intervals. The two largest alleles (160 and 165 bp) were observed only in males, which suggests that they were amplified from the Y chromosome DXYS156Y locus. The other 5 alleles were present in two copies in females and in a single copy in males, which suggests that they were amplified from the X chromosome DXYS156X locus. Locus DXYS156X was polymorphic in CEPH families with an observed heterozygosity in females of 46% (27 of 59). Linkage analysis with DNA markers on the X chromosome revealed significant lod scores for a location of DXYS156X close to markers DXS1002 ( θ= 0.000; z = 8.43), DXYS1X (θ=0.015; z=17.3), DXS3, and PGK1 in the region of chromosome Xql3. The sequence of DXYS156Y derived from the 165 bp allele has been deposited in Genbank with accession number X71600. © 1994 Wiley‐Liss, Inc.
AB - We report the isolation and characterization of a polymorphic pentanucleotide repeat (TAAAA)n, which was mapped to human chromosomes X and Y (loci DXYS156X and DXYS156Y) by PCR amplification of DNA from a monochromosomal somatic cell hybrid panel (NIGMS panel 2). The (TAAAA)n repeat of loci DXYS156 occurs within a human LINE element at a position where the consensus sequence contains a single TAAAA motif. In 72 unrelated CEPH individuals seven alleles were detected which ranged in size from 125 to 165 bp in 5 bp intervals. The two largest alleles (160 and 165 bp) were observed only in males, which suggests that they were amplified from the Y chromosome DXYS156Y locus. The other 5 alleles were present in two copies in females and in a single copy in males, which suggests that they were amplified from the X chromosome DXYS156X locus. Locus DXYS156X was polymorphic in CEPH families with an observed heterozygosity in females of 46% (27 of 59). Linkage analysis with DNA markers on the X chromosome revealed significant lod scores for a location of DXYS156X close to markers DXS1002 ( θ= 0.000; z = 8.43), DXYS1X (θ=0.015; z=17.3), DXS3, and PGK1 in the region of chromosome Xql3. The sequence of DXYS156Y derived from the 165 bp allele has been deposited in Genbank with accession number X71600. © 1994 Wiley‐Liss, Inc.
KW - Chromosomes X, Y
KW - DNA polymorphisms
KW - Tetranucleotide repeat
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U2 - 10.1002/humu.1380040306
DO - 10.1002/humu.1380040306
M3 - Article
C2 - 7833950
AN - SCOPUS:0028099805
SN - 1059-7794
VL - 4
SP - 208
EP - 211
JO - Human Mutation
JF - Human Mutation
IS - 3
ER -