Determination and Regional Assignment of Grouped Sets of Microclones in Chromosome 1pter–p35

In an approach to mapping physically the most distal 30 Mb of human chromosome 1p, region-specific clone libraries were generated by microdissection and microcloning. PFGE blot hybridization of single or low-copy microclones against rare-cutter digests of genomic DNA revealed physical linkage for gr...

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Published inGenomics (San Diego, Calif.) Vol. 29; no. 3; pp. 607 - 615
Main Authors BARNAS, CHRISTOPH M., ONYANGO, PATRICK, ELLMEIER, WILFRIED, LENGAUER, CHRISTOPH, KLEINER, ELKE, HENN, TRAUDL, BRUNNER, CHRISTOPH, STAPLETON, PAULA, WEITH, ANDREAS
Format Journal Article
LanguageEnglish
Published San Diego, CA Elsevier Inc 10.10.1995
Elsevier
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Summary:In an approach to mapping physically the most distal 30 Mb of human chromosome 1p, region-specific clone libraries were generated by microdissection and microcloning. PFGE blot hybridization of single or low-copy microclones against rare-cutter digests of genomic DNA revealed physical linkage for groups of markers. Supplementary PFGE analysis of 31 1p36–p35-specific probes for genetically mapped loci established a total of 15 grouped sets, consisting of altogether 69 markers. Twelve of the grouped sets were located in 1pter–p36.12, as revealed by microcell hybrid mapping; the remaining three were localized proximal to 1p36.12. Regional assignment and ordering of most grouped sets was achieved either by evaluating the included genetic markers or by fluorescencein situhybridization of representative probes. The genomic extent of individual grouped sets encompassed between 1100 and 2100 kb, covering a total of approximately 22 Mb of the distal chromosome 1p region. One particular grouped set was shown to contain seven polymorphic marker loci that were previously suggested to be distributed across the entire 1pter–p35 region. The increase in the number of hybridization marker probes in 1p36 and their physical mapping is expected to facilitate positional cloning experiments in this region; in particular, the construction of clone contigs may be greatly facilitated.
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ISSN:0888-7543
1089-8646
DOI:10.1006/geno.1995.9006