scholarly journals Four Previously Identified Petunia inflata S-Locus F-Box Genes Are Involved in Pollen Specificity in Self-Incompatibility

2014 ◽  
Vol 7 (3) ◽  
pp. 567-569 ◽  
Author(s):  
Justin S. Williams ◽  
Christopher A. Natale ◽  
Ning Wang ◽  
Shu Li ◽  
Tarah R. Brubaker ◽  
...  
Genome ◽  
2000 ◽  
Vol 43 (5) ◽  
pp. 820-826 ◽  
Author(s):  
Andrew G McCubbin ◽  
Carmen Zuniga ◽  
Teh-hui Kao

The Solanaceae family of flowering plants possesses a type of self-incompatibility mechanism that enables the pistil to reject self pollen but accept non-self pollen for fertilization. The pistil function in this system has been shown to be controlled by a polymorphic gene at the S-locus, termed the S-RNase gene. The pollen function is believed to be controlled by another as yet unidentified polymorphic gene at the S-locus, termed the pollen S-gene. As a first step in using a functional genomic approach to identify the pollen S-gene, a genomic BAC (bacterial artificial chromosome) library of the S2S2 genotype of Petunia inflata, a self-incompatible solanaceous species, was constructed using a Ti-plasmid based BAC vector, BIBAC2. The average insert size was 136.4 kb and the entire library represented a 7.5-fold genome coverage. Screening of the library using cDNAs for the S2-RNase gene and 13 pollen-expressed genes that are linked to the S-locus yielded 51 positive clones, with at least one positive clone for each gene. Collectively, at least 2 Mb of the chromosomal region was spanned by these clones. Together, three clones that contained the S2-RNase gene spanned ~263 kb. How this BAC library and the clones identified could be used to identify the pollen S-gene and to study other aspects of self-incompatibility is discussed.Key words: bacterial artificial chromosome, Petunia inflata, pollen-pistil interactions, self-incompatibility, S-locus.


2001 ◽  
Vol 125 (2) ◽  
pp. 1012-1022 ◽  
Author(s):  
Xi Wang ◽  
Austin L. Hughes ◽  
Tatsuya Tsukamoto ◽  
Toshio Ando ◽  
Teh-Hui Kao

2014 ◽  
Vol 26 (7) ◽  
pp. 2873-2888 ◽  
Author(s):  
Justin S. Williams ◽  
Joshua P. Der ◽  
Claude W. dePamphilis ◽  
Teh-hui Kao

2004 ◽  
Vol 54 (5) ◽  
pp. 727-742 ◽  
Author(s):  
Yan Wang ◽  
Tatsuya Tsukamoto ◽  
Ki-wan Yi ◽  
Xi Wang ◽  
Shihshieh Huang ◽  
...  

Genome ◽  
2000 ◽  
Vol 43 (4) ◽  
pp. 619-627 ◽  
Author(s):  
Andrew G McCubbin ◽  
Xi Wang ◽  
Teh-hui Kao

Solanaceous type self-incompatibility (SI) is controlled by a single polymorphic locus, termed the S-locus. The only gene at the S-locus that has been characterized thus far is the S-RNase gene, which controls pistil function, but not pollen function, in SI interactions between pistil and pollen. One approach to identifying additional genes (including the pollen S-gene, which controls pollen function in SI) at the S-locus and to study the structural organization of the S-locus is chromosome walking from the S-RNase gene. However, the presence of highly repetitive sequences in its flanking regions has made this approach difficult so far. Here, we used RNA differential display to identify pollen cDNAs of Petunia inflata, a self-incompatible solanaceous species, which exhibited restriction fragment length polymorphism (RFLP) for at least one of the three S-haplotypes (S1, S2, and S3) examined. We found that the genes corresponding to 10 groups of pollen cDNAs are genetically tightly linked to the S-RNase gene. These cDNA markers will expedite the mapping and cloning of the chromosomal region of the Solanaceae S-locus by providing multiple starting points.Key words: Petunia inflata, pollen cDNAs, self-incompatibility, S-linked cDNA markers, S-locus.


Genetics ◽  
2000 ◽  
Vol 154 (1) ◽  
pp. 413-420 ◽  
Author(s):  
Makoto Kusaba ◽  
Masanori Matsushita ◽  
Keiichi Okazaki ◽  
Yoko Satta ◽  
Takeshi Nishio

Abstract Self-incompatibility (SI) is a mechanism for preventing self-fertilization in flowering plants. In Brassica, it is controlled by a single multi-allelic locus, S, and it is believed that two highly polymorphic genes in the S locus, SLG and SRK, play central roles in self-recognition in stigmas. SRK is a putative receptor protein kinase, whose extracellular domain exhibits high similarity to SLG. We analyzed two pairs of lines showing cross-incompatibility (S2 and S2-b; S13 and S13-b). In S2 and S2-b, SRKs were more highly conserved than SLGs. This was also the case with S13 and S13-b. This suggests that the SRKs of different lines must be conserved for the lines to have the same self-recognition specificity. In particular, SLG2-b showed only 88.5% identity to SLG2, which is comparable to that between the SLGs of different S haplotypes, while SRK2-b showed 97.3% identity to SRK2 in the S domain. These findings suggest that the SLGs in these S haplotypes are not important for self-recognition in SI.


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