CpG island libraries from human chromosomes 18 and 22: landmarks for novel genes

被引:25
作者
Cross, SH
Clark, VH
Simmen, MW
Bickmore, WA
Maroon, H
Langford, CF
Carter, NP
Bird, AP
机构
[1] Western Gen Hosp, MRC, Human Genet Unit, Edinburgh EH4 2XU, Midlothian, Scotland
[2] Univ Edinburgh, Inst Cell & Mol Biol, Edinburgh EH9 3JR, Midlothian, Scotland
[3] Sanger Ctr, Cambridge CB10 1SA, England
关键词
D O I
10.1007/s003350010071
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
CpG islands are found at the 5' end of approximately 60% of human genes and so are important genomic landmarks. They are concentrated in early-replicating, highly acetylated gene-rich regions. With respect to CpG island content, human Chrs 18 and 22 are very different from each other: Chr 18 appears to be CpG island poor, whereas Chr 22 appears to be CpG island rich. We have constructed and validated CpG island libraries from flow-sorted Chrs 18 and 22 and used these to estimate the difference in number of CpG islands found on these two chromosomes. These libraries contain normalized collections of sequences from the 5' end of genes. Clones from the libraries were sequenced and compared with the sequence databases; one third matched ESTs, thus anchoring these ESTs at the 5' end of their gene. However, it was striking that many clones either had no match or matched only existing CpG island clones. This suggests that a significant proportion of 5' gene sequences are absent from databases, presumably either because they are difficult to clone or the gene is poorly expressed and/or has a restricted expression pattern. This point should be taken into consideration if the currently available libraries are those used for the elucidation of complete, as opposed to partial, gene sequences. The Chr 18 and 22 CpG island libraries are a sequence resource for the isolation of such 5' gene sequences from specific human chromosomes.
引用
收藏
页码:373 / 383
页数:11
相关论文
共 36 条
[21]  
John RM, 1998, GENOME ANAL, V2, P217
[22]   BEWARE OF USING SMALL STATISTICAL SAMPLES WHEN ASSESSING THE QUALITY OF A DNA LIBRARY [J].
KOLLNER, M ;
GREULICH, KO .
GENOMICS, 1994, 23 (01) :185-191
[23]   Chicken microchromosomes are hyperacetylated, early replicating, and gene rich [J].
McQueen, HA ;
Siriaco, G ;
Bird, AP .
GENOME RESEARCH, 1998, 8 (06) :621-630
[24]   CpG islands of chicken are concentrated on microchromosomes [J].
McQueen, HA ;
Fantes, J ;
Cross, SH ;
Clark, VH ;
Archibald, AL ;
Bird, AP .
NATURE GENETICS, 1996, 12 (03) :321-324
[25]   CpG islands of the pig [J].
McQueen, HA ;
Clark, VH ;
Bird, AP ;
Yerle, M ;
Archibald, AL .
GENOME RESEARCH, 1997, 7 (09) :924-931
[26]   PARAMETERS OF THE HUMAN GENOME [J].
MORTON, NE .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (17) :7474-7476
[27]   MOLECULAR-CLONING OF A CDNA-ENCODING THE HUMAN SM-D AUTO-ANTIGEN [J].
ROKEACH, LA ;
HASELBY, JA ;
HOCH, SO .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (13) :4832-4836
[28]   A 1.7-MB YAC CONTIG AROUND THE HUMAN BDNF GENE (11P13) - INTEGRATION OF THE PHYSICAL, GENETIC, AND CYTOGENETIC MAPS IN RELATION TO WAGR SYNDROME [J].
ROSIER, MF ;
GOGUEL, AF ;
MARTIN, A ;
LEPASLIER, D ;
COUILLIN, P ;
HOULGATTE, R ;
BERNHEIM, A ;
AUFFRAY, C ;
DEVIGNES, MD .
GENOMICS, 1994, 24 (01) :69-77
[29]  
ROSS MT, 1997, GENOME MAPPING, P165
[30]   Identification of the gene-richest bands in human prometaphase chromosomes [J].
Saccone, S ;
Federico, C ;
Solovei, I ;
Croquette, MF ;
Della Valle, G ;
Bernardi, G .
CHROMOSOME RESEARCH, 1999, 7 (05) :379-386