Using the genomic DNAs of maize and rice as probes respectively, the homology of maize and rice genomes was assessed by genomic in situ hybridization. When rice genomic DNAs were hybridized to maize, all chromosomes d...Using the genomic DNAs of maize and rice as probes respectively, the homology of maize and rice genomes was assessed by genomic in situ hybridization. When rice genomic DNAs were hybridized to maize, all chromosomes displayed many multiple discrete regions, while each rice chromosome delineated a single consecutive chromosomal region after they were hybridized with maize genomic DNAs. The results indicate that the genomes of maize and rice share high homology, and confirm the proposal that maize and rice are diverged from a common ancestor.展开更多
The copy number of 5S rDNA and centromerie sequence RCS2 was determined by extended DNA fiber based fluorescence in situ hybridization (Fiber-FISH) in rice (Oryza sativa ssp. indica cv. Guangluai No. 4) genome. In ord...The copy number of 5S rDNA and centromerie sequence RCS2 was determined by extended DNA fiber based fluorescence in situ hybridization (Fiber-FISH) in rice (Oryza sativa ssp. indica cv. Guangluai No. 4) genome. In order to determine the copy number, it is necessary to know the basepair number that a given length DNA fiber contains under a microscope. Therefore, the length of two DNA frag-ments, in which the basepair number had been already known, was measured. The insert sequence of the tested BAC 38D17 was 136 kb and its extended DNA was 56.4 μm long, 2.41 kb/μm on average, while that of the tested BAC 44B4 was 144.5 kb in total and 55.7 μm long, 2.60 kb/μm on average under the microscope. They were very close to the theoretical value of B-DNA in the Watson-Crick DNA model, which is 2.97 kb/μm. According to the average value of basepair number per μm of the two samples mentioned above, that is, 2.51 kb/μm, it could be estimated that the copy number was about 686 for 5S rDNA and 286-1121 for the展开更多
In recent years, great progress has been made constantly in oil and gas exploration in the Lungudong region of the Tarim Basin. However, progress has been slow in the evaluation of its main oil-producing horizons -- t...In recent years, great progress has been made constantly in oil and gas exploration in the Lungudong region of the Tarim Basin. However, progress has been slow in the evaluation of its main oil-producing horizons -- the Ordovician carbonate reservoir beds. Based on previous researches and on the various data such as drilling, geology and oil test, in combination with the interpretation of each single-well imaging and conventional logging data, and through analysis and comparison, the identification methods in imaging and conventional logging for four types of carbonate reservoir beds in this region are summarized in this paper. Calculation formulas for four reservoir bed parameters, i. e. shale content, porosity, permeability and oil saturation in this region are proposed; and reservoir beds in this region are divided into three levels （Ⅰ, Ⅱ and Ⅲ） by combining oil test data and logging data, The lower limits of the effective porosity of reservoir beds and the fracture porosity of effective reservoir beds are determined as 1.8% and 0.04%, respectively. The physical property parameters are calculated by conventional logging curves, and the most advantageous areas for reservoir development are predicted comprehensively. On the plane, the high-value zones of reservoir bed parameters are mainly concentrated in the N-S-trending strike-slip fault, the Sangtamu fault horst zone and near the LG38 well area; vertically, the reservoir bed parameters of the Yijianfang Formation are better than those of the Yingshan and Lianglitage formations.展开更多
A simple novel protocol suitable for in situ detection of apoptotic plant cell death is presented. This protocol combines the chromosome spreading technique with an extended in situ end labeling version for plants and...A simple novel protocol suitable for in situ detection of apoptotic plant cell death is presented. This protocol combines the chromosome spreading technique with an extended in situ end labeling version for plants and makes it possible to detect apoptosis directly at chromosome,nuclear and DNA levels simultaneously with high-sensitivity. False positive and nonspecific signals can be efficiently avoided. Moreover, the changes of chromosomes, nuclei and DNA during the process of apoptosis can be characterized in situ. To illustrate this method, salt stress-induced cell death has been investigated in maize root meristematic cells.展开更多
基金the National NaturalScience Foundation of China (Grant No. 39870423) and the Doctorate Spot Fund of the Ministry of Education (Grant No. 207980112).
文摘Using the genomic DNAs of maize and rice as probes respectively, the homology of maize and rice genomes was assessed by genomic in situ hybridization. When rice genomic DNAs were hybridized to maize, all chromosomes displayed many multiple discrete regions, while each rice chromosome delineated a single consecutive chromosomal region after they were hybridized with maize genomic DNAs. The results indicate that the genomes of maize and rice share high homology, and confirm the proposal that maize and rice are diverged from a common ancestor.
基金This work was supported by the National Natural Science Foundation of China (Grant No. 39900083) the Research Fund of the Doctoral Program of Higher Education (Grant No. 207980112).
文摘The copy number of 5S rDNA and centromerie sequence RCS2 was determined by extended DNA fiber based fluorescence in situ hybridization (Fiber-FISH) in rice (Oryza sativa ssp. indica cv. Guangluai No. 4) genome. In order to determine the copy number, it is necessary to know the basepair number that a given length DNA fiber contains under a microscope. Therefore, the length of two DNA frag-ments, in which the basepair number had been already known, was measured. The insert sequence of the tested BAC 38D17 was 136 kb and its extended DNA was 56.4 μm long, 2.41 kb/μm on average, while that of the tested BAC 44B4 was 144.5 kb in total and 55.7 μm long, 2.60 kb/μm on average under the microscope. They were very close to the theoretical value of B-DNA in the Watson-Crick DNA model, which is 2.97 kb/μm. According to the average value of basepair number per μm of the two samples mentioned above, that is, 2.51 kb/μm, it could be estimated that the copy number was about 686 for 5S rDNA and 286-1121 for the
基金supported by the State Key Development Program for Basic Research of China(Grant No.2006CB202308)
文摘In recent years, great progress has been made constantly in oil and gas exploration in the Lungudong region of the Tarim Basin. However, progress has been slow in the evaluation of its main oil-producing horizons -- the Ordovician carbonate reservoir beds. Based on previous researches and on the various data such as drilling, geology and oil test, in combination with the interpretation of each single-well imaging and conventional logging data, and through analysis and comparison, the identification methods in imaging and conventional logging for four types of carbonate reservoir beds in this region are summarized in this paper. Calculation formulas for four reservoir bed parameters, i. e. shale content, porosity, permeability and oil saturation in this region are proposed; and reservoir beds in this region are divided into three levels （Ⅰ, Ⅱ and Ⅲ） by combining oil test data and logging data, The lower limits of the effective porosity of reservoir beds and the fracture porosity of effective reservoir beds are determined as 1.8% and 0.04%, respectively. The physical property parameters are calculated by conventional logging curves, and the most advantageous areas for reservoir development are predicted comprehensively. On the plane, the high-value zones of reservoir bed parameters are mainly concentrated in the N-S-trending strike-slip fault, the Sangtamu fault horst zone and near the LG38 well area; vertically, the reservoir bed parameters of the Yijianfang Formation are better than those of the Yingshan and Lianglitage formations.
文摘A simple novel protocol suitable for in situ detection of apoptotic plant cell death is presented. This protocol combines the chromosome spreading technique with an extended in situ end labeling version for plants and makes it possible to detect apoptosis directly at chromosome,nuclear and DNA levels simultaneously with high-sensitivity. False positive and nonspecific signals can be efficiently avoided. Moreover, the changes of chromosomes, nuclei and DNA during the process of apoptosis can be characterized in situ. To illustrate this method, salt stress-induced cell death has been investigated in maize root meristematic cells.
