Abstract
Three alleles of the self-incompatibility gene of Nicotiana alata have been cloned and sequenced. A comparison of the sequences shows a surprisingly low level of homology (56%) and the presence of defined regions of homology and variability. The homologous regions include the N-terminal sequence, most of the cysteine residues and glycosylation sites, as well as other blocks throughout the sequence. We interpret these conserved regions as "framework" and nonconserved regions as "hypervariable," following the terminology used to describe analogous regions in the IgG supergene family. The low level of overall homology forms the basis of a general method for isolating S-allele-specific cDNAs. Allele-specific antibodies can be generated using synthetic peptides corresponding to one of the variable regions. When applied to sections of the pistil, these antibodies label the intercellular matrix in the stigma and transmitting tissue of the style and the cell walls in the epidermis of the placenta. HindIII digestion of genomic DNA generates a characteristic pattern of S-gene fragments for each genotype. These restriction fragment length polymorphisms can be used to assign S-genotype to progeny arising from breeding experiments.
MeSH Terms
Alleles
Amino Acid Sequence
Antibodies/immunology
Cloning, Molecular
Genetic Variation
Genotype
Glycoproteins/genetics
Immunohistochemistry
Microscopy, Electron
Molecular Sequence Data
Plant Proteins/genetics
Plants, Toxic
Pollen/physiology
Reproduction/genetics
Sequence Homology, Nucleic Acid
Tobacco/genetics,ultrastructure
Chemicals
Antibodies
Glycoproteins
Plant Proteins
self-incompatibility glycoprotein, Nicotiana
Authors & Affiliations
9 authors, click to expand affiliations / ORCID
Anderson M A
Plant Cell Biology Research Centre, School of Botany, University of Melbourne, Parkville, Victoria, Australia.
McFadden G I
Bernatzky R
Atkinson A
Orpin T
Dedman H
Tregear G
Fernley R
Clarke A E
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