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Molecular characterization and evolution of self-incompatibility genes in Arabidopsis thaliana: the case of the Sc haplotype. | LitMetric

AI Article Synopsis

  • The shift from outcrossing to self-fertility in Arabidopsis thaliana is linked to mutations in key genes (SRK and SCR) that determine self-incompatibility.
  • Research focused on the lesser-known SC haplotype reveals its SCRC gene but indicates its genes are nonfunctional, which is significant for understanding self-fertility.
  • The study also identifies specific mutations causing gene inactivation, contributing to broader insights into S-locus mechanisms in A. thaliana.

Article Abstract

The switch from an outcrossing mode of mating enforced by self-incompatibility to self-fertility in the Arabidopsis thaliana lineage was associated with mutations that inactivated one or both of the two genes that comprise the self-incompatibility (SI) specificity-determining S-locus haplotype, the S-locus receptor kinase (SRK) and the S-locus cysteine-rich (SCR) genes, as well as unlinked modifier loci required for SI. All analyzed A. thaliana S-locus haplotypes belong to the SA, SB, or SC haplotypic groups. Of these three, the SC haplotype is the least well characterized. Its SRKC gene can encode a complete open-reading frame, although no functional data are available, while its SCRC sequences have not been isolated. As a result, it is not known what mutations were associated with inactivation of this haplotype. Here, we report on our analysis of the Lz-0 accession and the characterization of its highly rearranged SC haplotype. We describe the isolation of its SCRC gene as well as the subsequent isolation of SCRC sequences from other SC-containing accessions and from the A. lyrata S36 haplotype, which is the functional equivalent of the A. thaliana SC haplotype. By performing transformation experiments using chimeric SRK and SCR genes constructed with SC- and S36-derived sequences, we show that the SRKC and SCRC genes of Lz-0 and at least a few other SC-containing accessions are nonfunctional, despite SCRC encoding a functional full-length protein. We identify the probable mutations that caused the inactivation of these genes and discuss our results in the context of mechanisms of S-locus inactivation in A. thaliana.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3584011PMC
http://dx.doi.org/10.1534/genetics.112.146787DOI Listing

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