Four polymorphic markers on rat chromosome 12 form a single linkage group

1993 ◽  
Vol 31 (9-10) ◽  
pp. 441-448 ◽  
Author(s):  
Peter Mathern ◽  
Ellen A. Goldmuntz ◽  
Hongbin Zha ◽  
Ying Du ◽  
Leslie J. Crofford ◽  
...  
Keyword(s):  
Linkage Group ◽  
Chromosome 12 ◽  
Polymorphic Markers ◽  
Single Linkage

scholarly journals Genetic map of seven polymorphic markers comprising a single linkage group on rat Chromosome 5

1993 ◽  
Vol 4 (11) ◽  
pp. 670-675 ◽  
Author(s):  
Ellen A. Goldmuntz ◽  
Elaine F. Remmers ◽  
Hongbin Zha ◽  
Peter Mathern ◽  
Ying Du ◽  
...  
Keyword(s):  
Linkage Group ◽  
Genetic Map ◽  
Polymorphic Markers ◽  
Chromosome 5 ◽  
Single Linkage

A single linkage group comprising 11 polymorphic DNA markers on rat Chromosome 3

1994 ◽  
Vol 5 (9) ◽  
pp. 538-541 ◽  
Author(s):  
H. Zha ◽  
E. F. Remmers ◽  
Y. Du ◽  
E. A. Goldmuntz ◽  
P. Mathern ◽  
...  
Keyword(s):  
Linkage Group ◽  
Dna Markers ◽  
Chromosome 3 ◽  
Single Linkage

scholarly journals Single linkage group per chromosome genetic linkage map for the horse, based on two three-generation, full-sibling, crossbred horse reference families

Genomics ◽  
2006 ◽  
Vol 87 (1) ◽  
pp. 1-29 ◽  
Author(s):  
June E. Swinburne ◽  
Mike Boursnell ◽  
Gemma Hill ◽  
Louise Pettitt ◽  
Twink Allen ◽  
...  
Keyword(s):  
Linkage Group ◽  
Linkage Map ◽  
Genetic Linkage ◽  
Genetic Linkage Map ◽  
Single Linkage ◽  
Full Sibling

scholarly journals Chromosomes XIV and XVII of Saccharomyces cerevisiae constitute a single linkage group.

1982 ◽  
Vol 2 (11) ◽  
pp. 1399-1409 ◽  
Author(s):  
S Klapholz ◽  
R E Esposito
Keyword(s):  
Saccharomyces Cerevisiae ◽  
Linkage Group ◽  
Mapping Method ◽  
Normal Chromosome ◽  
Tetrad Analysis ◽  
Single Linkage ◽  
Previous Evidence ◽  
The Right ◽  
Lines Of Evidence

We present several lines of evidence that chromosomes XIV and XVII of Saccharomyces cerevisiae are not independent chromosomes, but rather constitute a single linkage group. Studies which made use of a new mapping method based on the haploidization-without-recombination meiotic phenotype of the spoll mutant initially indicated that markers on chromosomes XIV and XVII were linked. Tetrad analysis was used to establish gene-gene distances, and a new chromosome XIV map incorporating markers originally assigned to chromosome XVII was derived. During the course of trisomic segregation studies, we discovered that a 2n + 2 homothallic diploid, originally believed to be tetrasomic for chromosome XVII (now XIV), carries two normal chromosome XIV homologs and two aberrant homologs which appear to be deficient for a large portion of the right arm of XIV. The previous evidence that established chromosome XVII as an independent linkage group is discussed in the light of these findings.

Genetic map of nine polymorphic loci comprising a single linkage group on rat chromosome 10: Evidence for linkage conservation with human chromosome 17 and mouse chromosome 11

Genomics ◽  
1992 ◽  
Vol 14 (3) ◽  
pp. 618-623 ◽  
Author(s):  
Elaine F. Remmers ◽  
Ellen A. Goldmuntz ◽  
Joseph M. Cash ◽  
Leslie J. Crofford ◽  
Barbara Misiewicz-Poltorak ◽  
...  
Keyword(s):  
Linkage Group ◽  
Human Chromosome ◽  
Mouse Chromosome ◽  
Genetic Map ◽  
Chromosome 17 ◽  
Chromosome 11 ◽  
Single Linkage ◽  
Human Chromosome 17 ◽  
Mouse Chromosome 11 ◽  
Linkage Conservation

scholarly journals SCNN1, an Epithelial Cell Sodium Channel Gene in the Conserved Linkage Group on Mouse Chromosome 6 and Human Chromosome 12

Genomics ◽  
1994 ◽  
Vol 24 (1) ◽  
pp. 185-186 ◽  
Author(s):  
Miriam H. Meisler ◽  
Lon L. Barrow ◽  
Cecilia M. Canessa ◽  
Bernard C. Rossier
Keyword(s):  
Epithelial Cell ◽  
Linkage Group ◽  
Human Chromosome ◽  
Sodium Channel ◽  
Mouse Chromosome ◽  
Chromosome 12 ◽  
Chromosome 6 ◽  
Channel Gene ◽  
Sodium Channel Gene

scholarly journals 232 LINKAGE RELATIONSHIPS OF ISOZYME AND MORPHOLOGICAL MARKERS IN INTERSPECIFIC CROSSES OF CHESTNUT

HortScience ◽  
1994 ◽  
Vol 29 (5) ◽  
pp. 462f-462
Author(s):  
Hongwen Huang ◽  
Fenny Dane ◽  
Joseph D. Norton
Keyword(s):  
Linkage Group ◽  
Gene Order ◽  
Castanea Dentata ◽  
American Chestnut ◽  
Interspecific Crosses ◽  
Marker Genes ◽  
Morphological Markers ◽  
Morphological Marker ◽  
Single Linkage ◽  
Linkage Relationships

Linkage relations among eight isozyme genes, Acp-3, Est-1, Est-5, Prx-1, Prx-2, Prx-3, Me and Adh, and two morphological markers, Inh, and Twh, were investigated in one F2 and two BC1 families of interspecific crosses between the American chestnut (Castanea dentata) and the Chinese chestnut (C. mollissima). Inh was found to be consistently linked with Prx-1 and Est-5 in all families. The order of these three genes was determined to be-Ihn--Prx1--Est5. In addition, four other gene pairs, Acp3--Inh, Acp3--Prx1, Me--Inh and Twh--Inh were found to be linked in one of the three families investigated. The four isozyme genes and two morphological marker genes were tentatively integrated into one linkage group with the following gene order Acp3--Me--Twh--Inh--Prx1-Est5. This study demonstrated that isozyme genes can be integrated with morphological marker genes into a single linkage map without the need for additional crosses.

An Amplified Fragment Length Polymorphism Map of the Silkworm

Genetics ◽  
2001 ◽  
Vol 157 (3) ◽  
pp. 1277-1284 ◽  
Author(s):  
Yuan-De Tan ◽  
Chunling Wan ◽  
Yufang Zhu ◽  
Chen Lu ◽  
Zhonghuai Xiang ◽  
...  
Keyword(s):  
Linkage Group ◽  
Linkage Map ◽  
Length Polymorphism ◽  
Fragment Length ◽  
Fragment Length Polymorphism ◽  
Amplified Fragment Length Polymorphism ◽  
Aflp Markers ◽  
Polymorphic Markers ◽  
Linkage Groups ◽  
Group 3

Abstract The silkworm (Bombyx mori L.) is a lepidopteran insect with a long history of significant agricultural value. We have constructed the first amplified fragment length polymorphism (AFLP) genetic linkage map of the silkworm B. mori at a LOD score of 2.5. The mapping AFLP markers were genotyped in 47 progeny from a backcross population of the cross no. 782 × od100. A total of 1248 (60.7%) polymorphic AFLP markers were detected with 35 PstI/TaqI primer combinations. Each of the primer combinations generated an average of 35.7 polymorphic AFLP markers. A total of 545 (44%) polymorphic markers are consistent with the expected segregation ratio of 1:1 at the significance level of P = 0.05. Of the 545 polymorphic markers, 356 were assigned to 30 linkage groups. The number of markers on linkage groups ranged from 4 to 36. There were 21 major linkage groups with 7-36 markers and 9 relatively small linkage groups with 4-6 markers. The 30 linkage groups varied in length from 37.4 to 691.0 cM. The total length of this AFLP linkage map was 6512 cM. Genetic distances between two neighboring markers on the same linkage group ranged from 0.2 to 47 cM with an average of 18.2 cM. The sex-linked gene od was located between the markers P1T3B40 and P3T3B27 at the end of group 3, indicating that AFLP linkage group 3 was the Z (sex) chromosome. This work provides an essential basic map for constructing a denser linkage map and for mapping genes underlying agronomically important traits in the silkworm B. mori L.

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