REFINEMENT OF THE LOCALIZATION OF THE GENE FOR HUMAN INTRAACROSOMAL PROTEIN SP-10 (ACRV1) TO THE JUNCTION OF BANDS Q23 -] Q24 OF CHROMOSOME-11 BY NONISOTOPIC IN-SITU HYBRIDIZATION

被引:13
作者
GOLDEN, WL
VONKAPHERR, C
KURTH, B
WRIGHT, RM
FLICKINGER, CJ
EDDY, R
SHOWS, T
HERR, JC
机构
[1] UNIV VIRGINIA,HLTH SCI CTR,DEPT ANAT,CHARLOTTESVILLE,VA 22908
[2] UNIV VIRGINIA,HLTH SCI CTR,DEPT CELL BIOL,CHARLOTTESVILLE,VA 22908
[3] UNIV VIRGINIA,HLTH SCI CTR,CTR RECOMBINANT GAMETE CONTRACEPT VACCINOGENS,CHARLOTTESVILLE,VA 22908
[4] ROSWELL PK MEM INST,DEPT HUMAN GENET,BUFFALO,NY
关键词
D O I
10.1006/geno.1993.1496
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The human sperm antigen SP-10 is a testis-specific protein associated with the real matrix of the acrosomal vesicle in developing spermatids and the acrosomal matrix and membranes of ejaculated sperm. A previous study, utilizing somatic cell hybrids, localized the gene for SP-10 to chromosome 11 and assigned the gene symbol ACRV1 (acrosomal vesicle protein-1). Although previous analysis of several somatic cell hybrids containing portions of chromosome 11 indicated that ACRV1 was in the p12 → q13 region, the present fluorescence in situ hybridization studies using cDNA, ribo, and genomic versions of probes for SP-10 coupled to analysis of an expanded series of somatic cell hybrids demonstrated the refined localization of ACRV1 to the junction of bands q23 and q24 of chromosome 11. A comparison of the three types of probes used for the in situ study demonstrated that while the genomic probe hybridized most efficiently, the riboprobe hybridized to the same location and was superior to the cDNA probe in mapping this single-copy gene. This report emphasizes the utility of riboprobes for chromosome localization of single-copy genes. © 1993 Academic Press. All rights reserved.
引用
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页码:446 / 449
页数:4
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