Bacterial contig map of the 21q11 region associated with Alzheimer's disease and abnormal myelopoiesis in Down syndrome

被引:19
作者
Groet, J
Ives, JH
South, AP
Baptista, PR
Jones, TA
Yaspo, ML
Lehrach, H
Potier, MC
Van Broeckhoven, C
Nizetic, D
机构
[1] Univ London, Sch Pharm, Ctr Appl Mol Biol, London WC1N 1AX, England
[2] Imperial Canc Res Fund, Human Cytogenet Lab, London WC2A 3PX, England
[3] Max Planck Inst Human Genet, Berlin, Germany
[4] CNRS, Neurobiol Lab, URA 2054, F-75005 Paris, France
[5] Univ Antwerp VIB, Dept Biochem, Born Bunge Fdn, Lab Neurogenet, B-2020 Antwerp, Belgium
关键词
D O I
10.1101/gr.8.4.385
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We present a high-resolution bacterial contig map of 3.4 Mb of genomic DNA in human chromosome 21q11-q21, encompassing the region of elevated disomic homozygosity in Down Syndrome-associated abnormal myelopoiesis and leukemia, as well as the markers, which has shown a strong association with Alzheimer's Disease that has never been explained. The map contains 89 overlapping PACs, BACs, or cosmids in three contigs (850, 850, and 1500 kb) with two gaps (one of 140-210 kb and the second <5 kb). To date, eight transcribed sequences derived by cDNA selection, exon trapping, and/or global EST sequencing have been positioned onto the map, and the only two genes so far mapped to this cytogenetic region, STCH and RIP140 have been precisely localized. This work converts a further 10% of chromosome 21q into a high-resolution bacterial contig map, which will be the physical basis for the long-range sequencing of this region. The map will also enable positional derivation of new transcribed sequences, as well as new polymorphic probes, that will help in elucidation of the role the genes in this region may play in abnormal myelopoiesis and leukemia associated with trisomy 21 and Alzheimer's Disease.
引用
收藏
页码:385 / 398
页数:14
相关论文
共 61 条
[1]  
ABE K, 1989, HUM GENET, V82, P313
[2]  
ANAND R, 1995, DNA CLONING, V3, P103
[3]  
Antonarakis S E, 1989, Prog Clin Biol Res, V311, P29
[4]   THE DIRECT SCREENING OF COSMID LIBRARIES WITH YAC CLONES [J].
BAXENDALE, S ;
BATES, GP ;
MACDONALD, ME ;
GUSELLA, JF ;
LEHRACH, H .
NUCLEIC ACIDS RESEARCH, 1991, 19 (23) :6651-6651
[5]   Localization of STCH to human chromosome 21q11.1 [J].
Brodsky, G ;
Otterson, GA ;
Parry, BB ;
Hart, I ;
Patterson, D ;
Kaye, FJ .
GENOMICS, 1995, 30 (03) :627-628
[6]   NUCLEAR FACTOR RIP140 MODULATES TRANSCRIPTIONAL ACTIVATION BY THE ESTROGEN-RECEPTOR [J].
CAVAILLES, V ;
DAUVOIS, S ;
LHORSET, F ;
LOPEZ, G ;
HOARE, S ;
KUSHNER, PJ ;
PARKER, MG .
EMBO JOURNAL, 1995, 14 (15) :3741-3751
[7]   Cloning of 559 potential exons of genes of human chromosome 21 by exon trapping [J].
Chen, H ;
Chrast, R ;
Rossier, C ;
Morris, MA ;
Lalioti, MD ;
Antonarakis, SE .
GENOME RESEARCH, 1996, 6 (08) :747-760
[8]   ISOLATION AND MAPPING OF HUMAN-CHROMOSOME-21 CDNA - PROGRESS IN CONSTRUCTING A CHROMOSOME-21 EXPRESSION MAP [J].
CHENG, JF ;
BOYARTCHUK, V ;
ZHU, YW .
GENOMICS, 1994, 23 (01) :75-84
[9]   EXPRESSED SEQUENCE TAGS FROM THE LONG ARM OF HUMAN-CHROMOSOME-21 [J].
CHIANG, PW ;
DZIDA, G ;
GRUMET, J ;
CHENG, JF ;
SONG, WJ ;
CROMBEZ, E ;
VANKEUREN, ML ;
KURNIT, DM .
GENOMICS, 1995, 29 (02) :383-389
[10]  
CHOO KH, 1990, MOL BIOL MED, V7, P437