scholarly journals AFFINITY DISTANCE VALUES AMONG SOMATIC METAPHASE CHROMOSOMES IN MAIZE

Genetics ◽  
1978 ◽  
Vol 88 (1) ◽  
pp. 181-199
Author(s):  
J D Horn ◽  
D B Walden

ABSTRACT In maize root-tip metaphase preparations, all distances between two chromosomes were measured in 50 cells from each of seven stocks and in 30 from one stock; four were arrested with cold, two with 8-hydroxyquinoline, one with colchicine and one with monobromonaphthalene Standardized, affinity-distance values were calculated for all pairs of homologues and pairs of nonhomologues from each preparation. The homologues of pair X were the least separated, those of pair I the most separated in the cold-arrested stocks. All but pairs I and VIII were shown to be significantly different from the observed mean. The observed mean was less than but not significantly different from the theoretical value for a random distribution. The use of chemical agents for metaphase arrest increased the separation of homologues, except for pair I.—Eleven percent of the comparisons of nonhomologues from cold-arrested, as contrasted to none of the comparisons from the c-metaphase treatments, were significantly different from the theoretical talue for a random distribution. This was considered evidence for limited primary nonhomologue association in maize. Although there were specific, differential responses to the two arrest agents, the population of homologous pairs approached a random distribution only in chemically arrested stocks.—Primary homologue association was considered to be maintained by two mechanisms. the more common involving the micro-tubules and the second involving the nucleolus.—Interpretations are offered regarding the claims of somatic association in other species, especially man. The opportunity in maize for experimentally modifying distance values by cytogenetic techniques is discussed.

Genome ◽  
1996 ◽  
Vol 39 (4) ◽  
pp. 697-703 ◽  
Author(s):  
Jai-Heon Lee ◽  
K. Arumuganathan ◽  
S. M. Kaeppler ◽  
C. M. Papa ◽  
H. F. Kaeppler

Accumulation of cells containing metaphase chromosomes is an important step in cytological analyses and chromosome sorting procedures. The goal of this research was to optimize treatment parameters to synchronize the cell cycle of maize root tip meristem cells. Levels of hydroxyurea, a DNA synthesis inhibitor, were assessed for their utility in accumulating cells at the G1 phase of the cell cycle. Trifluralin, amiprophos-methyl, and colchicine were used to accumulate cells containing metaphase chromosomes upon release from hydroxyurea inhibition. Optimal mitotic indices were achieved by treating seedlings with 5 mM hydroxyurea for 18 h, incubating for 1 h without chemical treatment to release the hydroxyurea block, and then treating emerging roots with 1 μM trifluralin for 4 h. The mitotic index of synchronized maize root tips was over 70%. Uniformity of synchronization depended upon selection of seeds with emerging radicles that were similar in length at the time of treatment. Suspensions of intact chromosomes were prepared by a simple slicing procedure. The chromosome preparations were found to be suitable for flow cytometric characterization and sorting. Chromosome peaks of the observed flow karyotype resembled the predicted flow karyotype calculated on the basis of maize chromosome size. Key words : flow karyotype, hydroxyurea, plant chromosome sorting, trifluralin.


1950 ◽  
Author(s):  
Gabriel Baldovinos de la Pena
Keyword(s):  

1993 ◽  
Vol 125 (2) ◽  
pp. 413-429 ◽  
Author(s):  
R. M. ABEYSEKERA ◽  
M. E. McCULLY

1963 ◽  
Vol 19 (1) ◽  
pp. 59-69 ◽  
Author(s):  
M. Choraży ◽  
A. Bendich ◽  
E. Borenfreund ◽  
D. J. Hutchison

A method for the isolation of metaphase chromosomes from mouse L1210 leukemia cells has been developed. Cells, arrested at metaphase with colchicine, were exposed to hypotonic solution and the pH was then adjusted to 5.6 to stabilize the chromosomes. The metaphase figures were subsequently disrupted and the chromosomes isolated by a series of differential centrifugations in sucrose. The isolated chromosomes were well preserved, as judged by morphological criteria. The effect of various enzymes and chemical agents on the isolated chromosomes was studied. Chymotrypsin, trypsin, and deoxyribonuclease caused a marked disintegration of the chromosomes, whereas treatment with pepsin and ribonuclease induced no significant morphological alterations.


Genome ◽  
1992 ◽  
Vol 35 (4) ◽  
pp. 551-559 ◽  
Author(s):  
S. M. Albini ◽  
T. Schwarzacher

Surface-spread pollen mother cells at meiotic prophase from Secale cereale (rye) were used for fluorescent DNA:DNA in situ localization of two tandemly repeated DNA sequences: pTa71, a wheat rDNA clone, and pSc119.2, a cloned 120-bp repeat from rye heterochromatin. The fluorescent hybridization signal, consisting of many yellow-green dots, was closely associated with the bivalent axes, corresponding to the synaptonemal complex, and located in the surrounding chromatin. The rDNA signal was associated with one bivalent, the smallest of the seven, at a distance about 13% of the bivalent length from the telomere. This corresponded to the position of the nucleolar organizing region of silver-stained synaptonemal complexes analyzed under the electron microscope and published data for somatic metaphase chromosomes. The relative length of the axis covered with the rDNA signal is less than expected from somatic metaphases, but it corresponds more closely to the proportion of the sequences in the genome. The hybridization signal with the 120-bp repeat was located mainly at the telomeric regions of several bivalents that showed thickenings of the axis after DAPI staining, probably corresponding to somatic C-bands. These major and some minor intercalary sites agree with the distribution of the 120-bp repeat in somatic metaphase. Fluorescent in situ hybridization to plant surface-spread pachytene chromosomes, which can be obtained in large numbers, has great potential for studying meiotic prophase, high-resolution mapping of DNA sequences, and investigating the relationship of DNA sequences to the synaptonemal complex.Key words: in situ hybridization, cereals, pachytene, meiosis, synaptonemal complex, physical mapping.


1968 ◽  
Vol 10 (2) ◽  
pp. 433-443 ◽  
Author(s):  
Ira H. Ames ◽  
Jyotirmay Mitra

Several approaches were employed to study the distribution of heterochromatin in root tip chromosomes of Haplopappus gracilis. Cold treatment and pretreatment in an aqueous solution of 8-hydroxyquinoline revealed achromatic gaps in metaphase chromosomes. Cold treatment also permitted the demonstration of positive heteropycnosis in prophase chromosomes. Further support for the identification of heterochromatic segments was provided by a study of the localization of chromosome aberrations induced by maleic hydrazide and an analysis of the pattern of DNA synthesis in chromosomes of root tip cells. Seven of the ten regions that were preferentially broken by maleic hydrazide also reacted differentially to cold treatment or to pretreatment with 8-hydroxyquinoline. A good correlation was found between regions that completed DNA replication late in the DNA-synnhetic period and segments that were shown to be heterochromatic by the other techniques.


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