A Sequence-Tagged Site Map of Human Chromosome 11

Smith, Michael W.; Clark, Stephen P.; Hutchinson, J; Wei, Yalin H.; Churukian, Allan C.; Daniels, Lori B.; Diggle, Karin; Gen, Michael W.; Romo, Anthony; Lin, Ying; Selleri, Licia; McElligott, David L.; Evans, Glen A.

doi:10.1006/geno.1993.1392

Cited by 50 publications

(23 citation statements)

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“…YAC libraries were screened with the microsatellite markers DllS861, DllS419, DllS902, DllS921, DllS1310, DllS899, and the STS 966e8(L) using a PCRbased library pooling strategy as described by Green and Olsen (1990). Primer sequences for the six microsatellite markers were obtained from Genome Data Base and Smith et al (1993). Oligonucleotide sequences for the STS 966e8(L) are shown in Table 1.…”

Section: Genome Research ~ 511mentioning

confidence: 99%

Construction of a YAC contig encompassing the Usher syndrome type 1C and familial hyperinsulinism loci on chromosome 11p14-15.1.

Ayyagari¹,

Nestorowicz²,

Li³

et al. 1996

Genome Res.

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The Usher syndrome type IC {USHIC} and familial hyperinsulinism [HI) loci have been assigned to chromosome Ilpl4-15.1, within the interval DIIS419-DI1SI310. We have constructed a yeast artificial chromosome {YAC} contig, extending from D11S926 to DIIS899, which encompasses the critical regions for both USHIC and HI and spans an estimated genetic distance of ---4 cM. A minimal set of six YAC clones constitute the contig, with another 22 YACs confirming the order of sequence-tagged sites [STSs) and position of YACs on the contig. A total of 40 STSs, including 10 new STSs generated from YAC insert-end sequences and inter-A/u PCR products, were used to order the clones within the contig. This physical map provides a resource for identification of gene transcripts associated with USHIC, HI, and other genetic disorders that map to the DllS?26-DIIS899 interval.

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Section: Genome Research ~ 511mentioning

confidence: 99%

Construction of a YAC contig encompassing the Usher syndrome type 1C and familial hyperinsulinism loci on chromosome 11p14-15.1.

Ayyagari¹,

Nestorowicz²,

Li³

et al. 1996

Genome Res.

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“…Our FISH data, using both normal meta phase chromosomes and chromosomes expressing the fragile site FRAl I A. clearly show a more distal assignment o f the PC locus, namely, I I q l3.4. compared with the region llqll-+ q 13.1 previously reported by Smith et al (1993).…”

mentioning

confidence: 49%

Assignment of the human pyruvate carboxylase gene (PC) to 11q13.4 by fluorescence in situ hybridisation

Walker

Baker

Wallace

et al. 1995

Cytogenet Genome Res

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“…PPP1CA, ACTN3, AHNAK, COX8 and NDUFV1 have been previously located on HSA11q13 (Barker et al, 1990;Beggs et al, 1992;Kudoh et al, 1995;Smith et al, 1993;Spencer et al, 1992) but not yet on the mouse genome. Although predictable from the syntenic conservation between HSA11q13 and MMU19 (Shows et al, 1996), their localization on this part of the mouse genome had to be established.…”

Section: Mapping Of Five New Mmu19 Genes (Type I Markers)mentioning

confidence: 98%

Comparative mapping of two adjacent regions of MMU19 with their human counterpart on HSA11q13

Fernandes

Lespinasse

Rotomondo

et al. 1998

Cytogenet Genome Res

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High resolution physical maps of two adjacent regions of MMU19 were constructed in order to establish a comparative map between the pericentromeric region of MMU19 and its human counterpart on HSA11q13. These two physical maps span 2.5 and 0.5 megabases on MMU19. Long range restriction analysis and YAC contigs have been built, five genes were located on MMU19 and eight new STSs were generated. The 0.5-Mb map which has been positioned close to the centromere of MMU19, based on dual-color FISH experiments and genetic data, includes eight genes (Type I markers), three microsatellites (Type II markers) and five new STSs. The 2.5-Mb map is located more telomeric and contains seven genes, four microsatellites and four new STSs. Gene order and physical distances appear to be similar in human and in mouse in this 2.5-Mb region. Strikingly, the 0.5-Mb region has a similar size in human but gene order is shuffled. The overall comparative map shows that these two regions are inverted on MMU19 when compared with HSA11q13.

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A Sequence-Tagged Site Map of Human Chromosome 11

Cited by 50 publications

References 0 publications

Construction of a YAC contig encompassing the Usher syndrome type 1C and familial hyperinsulinism loci on chromosome 11p14-15.1.

Construction of a YAC contig encompassing the Usher syndrome type 1C and familial hyperinsulinism loci on chromosome 11p14-15.1.

Assignment of the human pyruvate carboxylase gene (PC) to 11q13.4 by fluorescence in situ hybridisation

Comparative mapping of two adjacent regions of MMU19 with their human counterpart on HSA11q13

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