A RADIATION HYBRID MAP OF 95-STSS SPANNING HUMAN-CHROMOSOME 13Q

Citation
Sh. Shaw et al., A RADIATION HYBRID MAP OF 95-STSS SPANNING HUMAN-CHROMOSOME 13Q, Genomics, 27(3), 1995, pp. 502-510
Citations number
55
Categorie Soggetti
Genetics & Heredity
Journal title
ISSN journal
08887543
Volume
27
Issue
3
Year of publication
1995
Pages
502 - 510
Database
ISI
SICI code
0888-7543(1995)27:3<502:ARHMO9>2.0.ZU;2-1
Abstract
We have constructed a high-resolution physical map of the long arm of human chromosome 13 using a panel of 94 radiation hybrids. A comprehen sive map of 95 chromosome 13-specific sequence tagged sites (STSs) spa nning 13q from the presumed centromere at D13Z1 to the known telomere was obtained by multipoint maximum likelihood statistical methods. The 95 markers have an average retention frequency of 10%, with markers c loser to the centromere having much greater retention frequencies (22- 49%) than distal 13q markers (2-12%). The most likely radiation hybrid map localized the 95 STSs into 54 unique map positions, 34 with odds of 1000:1 or greater; the comprehensive map localized all but 17 STSs with odds exceeding 10:1. The total map length of 13q was 1302 cR(9000 ) (range 6.4-94.4 cR(9000)) and a physical distance of 98 Mb, so that 1% breakage in the RH panel corresponds to 75 kb. A comparison of the comprehensive RH map to genetic maps of chromosome 139 shows identical locus orders for the common markers, with two exceptions over 1-cM di stances. We discuss the possible relationships between the genetic and the radiation hybrid maps. (C) 1995 Academic Press, Inc.