Integrated cytogenetic map of mitotic metaphase chromosome 9 of maize: resolution, sensitivity, and banding paint development

被引:40
作者
Danilova, Tatiana V. [1 ]
Birchler, James A. [1 ]
机构
[1] Univ Missouri, Div Biol Sci, Columbia, MO 65211 USA
基金
美国国家科学基金会;
关键词
D O I
10.1007/s00412-008-0151-y
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
To study the correlation of the sequence positions on the physical DNA finger print contig (FPC) map and cytogenetic maps of pachytene and somatic maize chromosomes, sequences located along the chromosome 9 FPC map approximately every 10 Mb were selected to place on maize chromosomes using fluorescent in situ hybridization (FISH). The probes were produced as pooled polymerase chain reaction products based on sequences of genetic markers or repeat-free portions of mapped bacterial artificial chromosome (BAC) clones. Fifteen probes were visualized on chromosome 9. The cytological positions of most sequences correspond on the pachytene, somatic, and FPC maps except some probes at the pericentromeric regions. Because of unequal condensation of mitotic metaphase chromosomes, being lower at pericentromeric regions and higher in the arms, probe positions are displaced to the distal ends of both arms. The axial resolution of FISH on somatic chromosome 9 varied from 3.3 to 8.2 Mb, which is 12-30 times lower than on pachytene chromosomes. The probe collection can be used as chromosomal landmarks or as a "banding paint" for the physical mapping of sequences including transgenes and BAC clones and for studying chromosomal rearrangements.
引用
收藏
页码:345 / 356
页数:12
相关论文
共 57 条
[31]   Expanding the genetic map of maize with the intermated B73 x Mo17 (IBM) population [J].
Lee, M ;
Sharopova, N ;
Beavis, WD ;
Grant, D ;
Katt, M ;
Blair, D ;
Hallauer, A .
PLANT MOLECULAR BIOLOGY, 2002, 48 (05) :453-461
[32]   Physical mapping of 45S and 5S rDNA on maize metaphase and sorted chromosomes by FISH [J].
Li, LJ ;
Arumuganathan, K .
HEREDITAS, 2001, 134 (02) :141-145
[33]   Organization and variability of the maize genome [J].
Messing, J ;
Dooner, HK .
CURRENT OPINION IN PLANT BIOLOGY, 2006, 9 (02) :157-163
[34]   Gene duplication and exon shuffling by helitron-like transposons generate intraspecies diversity in maize [J].
Morgante, M ;
Brunner, S ;
Pea, G ;
Fengler, K ;
Zuccolo, A ;
Rafalski, A .
NATURE GENETICS, 2005, 37 (09) :997-1002
[35]  
Page BT, 2001, GENETICS, V159, P291
[36]   Ancient polyploidization predating divergence of the cereals, and its consequences for comparative genomics [J].
Paterson, AH ;
Bowers, JE ;
Chapman, BA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (26) :9903-9908
[37]   HIGHLY REPEATED DNA-SEQUENCE LIMITED TO KNOB HETEROCHROMATIN IN MAIZE [J].
PEACOCK, WJ ;
DENNIS, ES ;
RHOADES, MM ;
PRYOR, AJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1981, 78 (07) :4490-4494
[38]   Genome and chromosome identification in cultivated barley and related species of the Triticeae (Poaceae) by in situ hybridization with the GAA-satellite sequence [J].
Pedersen, C ;
Rasmussen, SK ;
LindeLaursen, I .
GENOME, 1996, 39 (01) :93-104
[39]  
Reeves A., 2000, MicroMeasure for Windows
[40]   Karyotype of maize (Zea mays L.) mitotic metaphase chromosomes as revealed by fluorescence in situ hybridization (FISH) with cytogenetic DNA markers [J].
Sadder, MT ;
Weber, G .
PLANT MOLECULAR BIOLOGY REPORTER, 2001, 19 (02) :117-123