Primary trisomics obtained from autotriploid by diploid reciprocal crosses in cucumber

2008 ◽  
Vol 22 (1) ◽  
pp. 45-51 ◽  
Author(s):  
Wei-Ping Diao ◽  
Sheng-You Bao ◽  
Biao Jiang ◽  
Li Cui ◽  
Jin-Feng Chen
Crop Science ◽  
1987 ◽  
Vol 27 (3) ◽  
pp. 435-439 ◽  
Author(s):  
I. Romagosa ◽  
L. Cistue ◽  
T. Tsuchiya ◽  
J. M. Lasa ◽  
R. J. Hecker
Keyword(s):  

Genetics ◽  
1996 ◽  
Vol 143 (1) ◽  
pp. 517-529
Author(s):  
Kuldeep Singh ◽  
D S Multani ◽  
Gurdev S Khush

Abstract Secondary trisomics and telotrisomics representing the 12 chromosomes of rice were isolated from the progenies of primary trisomics. A large population of each primary trisomic was grown. Plants showing variation in gross morphology compared to the primary trisomics and disomic sibs were selected and analyzed cytologically at diakinesis and pachytene. Secondary trisomics for both arms of chromosomes 1, 2, 6, 7 and 11 and for one arm of chromosomes 4, 5, 8, 9 and 12 were identified. Telotrisomics for short arm of chromosomes 1, 8, 9 and 10 and for long arms of chromosomes 2, 3 and 5 were isolated. These secondary and telotrisomics were characterized morphologically and for breeding behavior. Secondary trisomics 2n + 1S · 1S, 2n + 1L · 1L, 2n + 2S · 2S, 2n + 2L · 2L, 2n + 6S · 6S, 2n + 6L · 6L and 2n + 7L · 7L are highly sterile, and 2n + 1L · 1L, 2n + 2L · 2L and 2n + 7L · 7L do not set any seed even upon backcrossing. Telotrisomics are fertile and vigorous. Genetic segregation of 43 marker genes was studied in the F2 or backcross progenies. On the basis of segregation data, these genes were delimited to specific chromosome arms. Correct orientation of 10 linkage groups was determined and centromere positions on nine linkage groups were approximated. A revised linkage map of rice is presented.


Author(s):  
Ye Sol Jeong ◽  
Jae Kwang Kim ◽  
Seung-A. Baek ◽  
Jong-Yeol Lee ◽  
Dongho Lee ◽  
...  

1965 ◽  
Vol 45 (1) ◽  
pp. 33-36
Author(s):  
G. W. Rahnefeld

The relationship between thickness of fat measured at the shoulder, last rib, and loin of live pigs and market weight (86.2 to 95.2 kg) was studied in 1596 pigs from the Lacombe and Yorkshire breeds and their reciprocal crosses. No significant breed or sex differences were found in the proportion of fat at the three sites. Breed and sex differences were evident in the average depth of fat. The regression coefficients for the mean of three fat measurements on market weight were.016 ±.003,.019 ±.007, and.017 ±.004 for Lacombe males, barrows, and females respectively;.039 ±.002,.036 ±.005, and.041 ±.001 for Yorkshire males, barrows and females respectively;.027 ±.005 and.029 ±.004 for barrows and females from the Lacombe male × Yorkshire female mating; and.023 ±.007 and.021 ±.009 for barrows and females from the Yorkshire male × Lacombe female mating. Comparisons between animals measured at a relatively constant weight should be made after the fat measurement is adjusted for variations in body weight. The results of this study indicate that separate corrections should be applied for each breed. Separate corrections for sexes within breeds do not appear warranted.


1968 ◽  
Vol 10 (2) ◽  
pp. 263-275 ◽  
Author(s):  
K. Lesins ◽  
A. Erac

In crosses between the two taxa Medicago striata Bast, and M. littoralis Rohde a high mortality of gametes and seedlings, and sterility of some plants were noted which were not related to gross chromosomal rearrangements. Although the F1, F2 and F3 generations from reciprocal crosses differed in chlorophyll deficiencies (indicating a cytoplasmic influence) a genic cause became evident from segregations for chlorophyll characters in the F2 and F3. Transference of the cytoplasmic factor by the pollen is indicative.Segregation for pod coiling direction indicated that the character was determined by one or two genetic factors of which the clockwise coiling direction is recessive. The spininess appeared to be determined by one genetic factor, of which the spineless allele is recessive.On the basis of genetic differences (especially on the built-in repulsion systems for normal chlorophyll development of opposite species) the two taxa should be considered two different species.


1960 ◽  
Vol 39 (4) ◽  
pp. 876-881 ◽  
Author(s):  
Lloyd R. Champion

1982 ◽  
Vol 62 (2) ◽  
pp. 155-159 ◽  
Author(s):  
W. P. Bullock ◽  
P. S. Baenziger ◽  
G. W. Schaeffer ◽  
P. J. Bottino

2018 ◽  
Vol 59 (2) ◽  
pp. 193-201 ◽  
Author(s):  
D. A. T. Sutherland ◽  
C. F. Honaker ◽  
B. Dorshorst ◽  
L. Andersson ◽  
P. B. Siegel

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