Index, comprehensive microsatellite, and unified linkage maps of human chromosome 14 with cytogenetic tie points and a telomere microsatellite marker

Sunil D. Pandit, Jen C. Wang, Rosalie A. Veile, Santosh K. Mishra, Christopher A. Warlick, Helen Donis-Keller

Research output: Contribution to journalArticlepeer-review

13 Scopus citations

Abstract

Three sets of linkage maps (index, comprehensive microsatellite, and unified) have been constructed for human chromosome 14 based on genotypes from the CEPH reference pedigrees. The index maps consist of 18 microsatellite markers, with heterozygosities of at least 68% and intermarker spacing no greater than 11 cM. The sex-average comprehensive microsatellite map is 125 cM in length and includes 115 markers with 54 loci uniquely placed with odds for marker order of at least 1000:1. The sex-average index map length is 121 cM, and the female- and male-specific maps are 143 and 101 cM, respectively. A unified map was also constructed from 147 loci (162 marker systems), which includes 32 RFLP markers in addition to the 115 microsatellites. The sex-average length of the unified map is 128 cM with 69 loci uniquely placed. Our maps are anchored by a microsatellite telomere marker sCAW1 (D14S826), developed from a telomere YAC clone TYAC196, which extends the linkage map to the physical terminus of the long arm of chromosome 14. Furthermore, we have also physically mapped seven of the loci by fluorescencein situhybridization of cosmid clones orAlu-PCR products amplified from YACs containing the marker sequences. Together with previously established cytogenetic map designations for other loci, our maps display links between genetic markers for 10 of 13 cytogenetic bands of chromosome 14 at the 550 genome band resolution.

Original languageEnglish (US)
Pages (from-to)653-664
Number of pages12
JournalGenomics
Volume29
Issue number3
DOIs
StatePublished - Oct 1995

Bibliographical note

Funding Information:
We thank M. V. Olson and H. Riethman for providing the clone HTY2070/TYAC196 and cosmid subclones. This work was supported in part by NIH Grants HG-00469 and HG-00100 (to H.D-K).

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