A genetic linkage map for an apricot (Prunus armeniaca L.) BC1 population mapping plum pox virus resistance

2008 ◽  
Vol 4 (3) ◽  
pp. 481-493 ◽  
Author(s):  
D. A. Lalli ◽  
A. G. Abbott ◽  
T. N. Zhebentyayeva ◽  
M. L. Badenes ◽  
V. Damsteegt ◽  
...  
2019 ◽  
Vol 99 (5) ◽  
pp. 599-610
Author(s):  
Junhuan Zhang ◽  
Haoyuan Sun ◽  
Li Yang ◽  
Fengchao Jiang ◽  
Meiling Zhang ◽  
...  

A high-density genetic map of apricot (Prunus armeniaca L.) was constructed using an F1 population constructed by crossing two main Chinese cultivars ‘Chuanzhihong’ and ‘Luotuohuang’, coupled with a recently developed reduced representation library (RRL) sequencing. The average sequencing depth was 38.97 in ‘Chuanzhihong’ (female parent), 33.05 in ‘Luotuohuang’ (male parent), and 8.91 in each progeny. Based on the sequencing data, 12 451 polymorphic markers were developed and used in the construction of the genetic linkage map. The final map of apricot comprised eight linkage groups, including 1991 markers, and covered 886.25 cM of the total map length. The average distance between adjacent markers was narrowed to 0.46 cM. Gaps larger than 5 cM only accounted for <0.33%. To our knowledge, this map is the densest genetic linkage map that is currently available for apricot research. It is a valuable linkage map for quantitative trait loci (QTLs) identification of important agronomic traits. Moreover, the high marker density and well-ordered markers that this linkage map provides will be useful for molecular breeding of apricot as well. In this study, we applied this map in the QTL analysis of an important agronomic trait, pistil abortion. Several QTLs were detected and mapped respectively to the middle regions of LG5 (51.005∼59.4 cM) and LG6 (72.884∼76.562 cM), with nine SLAF markers closely linked to pistil abortion. The high-density genetic map and QTLs detected in this study will facilitate marker-assisted breeding and apricot genomic study.


2012 ◽  
Vol 38 (No. 2) ◽  
pp. 65-68 ◽  
Author(s):  
J. Salava ◽  
Y. Wang ◽  
B. Krška ◽  
J. Polák ◽  
P. Komínek ◽  
...  

A genetic linkage map for apricot (Prunus armeniaca L.) has been constructed using amplified fragment length polymorphism (AFLP) markers in 80 BC1&nbsp;individuals derived from a cross LE-3246 &times; Vestar. From 26 different primer combinations, a total of 248 AFLP markers were scored, of which, 40 were assigned to 8 linkage groups covering 315.8 cM of the apricot nuclear genome. The average interval between these markers was 7.7 cM. One gene (PPVres1) involved in resistance to PPV (Plum pox virus) was mapped. Two AFLP markers (EAA/MCAG8 and EAG/MCAT14) were found to be closely associated with the PPVres1 locus (4.6 cM resp. 4.7 cM). These markers are being characterized and they will be studied for utilization in apricot breeding with marker-assisted selection (MAS).


2009 ◽  
Vol 31 (6) ◽  
pp. 629-637 ◽  
Author(s):  
Wei-Dong LIU ◽  
Xiang-Bo BAO ◽  
Wen-Tao SONG ◽  
Zun-Chun ZHOU ◽  
Chong-Bo HE ◽  
...  

2016 ◽  
Vol 42 (2) ◽  
pp. 159 ◽  
Author(s):  
Jian-Bin GUO ◽  
Li HUANG ◽  
Liang-Qiang CHENG ◽  
Wei-Gang CHEN ◽  
Xiao-Ping REN ◽  
...  

2013 ◽  
Vol 19 (6) ◽  
pp. 930-938 ◽  
Author(s):  
Renyi PANG ◽  
Wentao SONG ◽  
Fengtao GAO ◽  
Xiaolin LIAO ◽  
Yongwei ZHAO ◽  
...  

Crop Science ◽  
2003 ◽  
Vol 43 (1) ◽  
pp. 367 ◽  
Author(s):  
Ju-Kyung Yu ◽  
Shunxue Tang ◽  
Mary B. Slabaugh ◽  
Adam Heesacker ◽  
Glenn Cole ◽  
...  

Genetics ◽  
2001 ◽  
Vol 158 (2) ◽  
pp. 695-700 ◽  
Author(s):  
David J Hawthorne

Abstract A genetic linkage map was constructed from an intraspecific cross of the Colorado potato beetle, Leptinotarsa decemlineata. This is an initial step toward mapping the loci that underlie important phenotypes associated with insect adaptation to an agroecosystem. The map was made with 172 AFLP and 10 anonymous codominant markers segregating among 74 backcross (BC1) individuals. Markers were mapped to 18 linkage groups and a subset of the markers with a mean intermarker distance of 11.1 cM is presented. A pyrethroid-resistance candidate gene, LdVssc1, was placed onto the map as well. The sex chromosome was identified by exploiting the XO nature of sex determination in this species using patterns of variation at LdVssc1 and the codominant markers.


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