Gene-based anchoring of the rat genetic linkage and cytogenetic mans: new regional localizations, orientation of the linkage groups, and insights into mammalian chromosome evolution

被引:50
作者
Szpirer, C
Szpirer, J
Van Vooren, P
Tissir, F
Simon, JS
Koike, G
Jacob, HJ
Lander, ES
Helou, K
Klinga-Levan, K
Levan, G
机构
[1] Free Univ Brussels, Dept Biol Mol, B-1640 Rhode St Genese, Belgium
[2] Massachusetts Gen Hosp, Cardiovasc Res Ctr, Charlestown, MA 02129 USA
[3] Harvard Univ, Sch Med, Charlestown, MA 02129 USA
[4] Med Coll Wisconsin, Dept Physiol, Milwaukee, WI 53226 USA
[5] MIT, Whitehead Inst Biomed Res, Cambridge, MA 02139 USA
[6] Univ Goteborg, CMB Genet, S-40530 Gothenburg, Sweden
关键词
D O I
10.1007/s003359900853
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
In order to generate anchor points connecting the rat cytogenetic and genetic maps, the cytogenetic position of 62 rat markers (including 55 genes) already localized genetically was determined by fluorescence in situ hybridization. Whenever possible, markers located near one end of the linkage groups were included. These new localizations allowed us to unambiguously orient the 20 autosomal and the X chromosome linkage groups. The position of the centromere in the linkage map could also be determined in the case of several metacentric chromosomes. In addition, the regional localization of 15 other rat genes was determined. These new data bring useful information with respect to comparative mapping with the mouse and the human and to mammalian evolution. They illustrate, for instance, that groups of genes can remain syntenic during mammalian evolution while being subjected to intrachromosomal rearrangements in some lineages (synteny is conserved while gene order is not:). This analysis also disclosed cases of synteny conservation in one the two rodent species and the human, while the synteny is split in the other rodent species: such configurations are likely examples of lineage-specific interchromosomal rearrangements associated with speciation.
引用
收藏
页码:721 / 734
页数:14
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