PolA2is required for embryo development inArabidopsisThis paper is one of a selection of papers published in a Special Issue from the National Research Council of Canada – Plant Biotechnology Institute.

Abstract

DNA replication machinery is highly conserved in eukaryotes. DNA polymerase is essential for the synthesis of new DNA strands and for DNA repair. Despite the significant progress in the understanding of these processes in yeast and animal model systems, there is only scant information available for their counterparts in plants. Among different multisubunit-containing DNA polymerases, DNA polymerase α (POLA complex) is composed of four subunits. In this study, we report on the characterization of PolA2, which encodes the putative B subunit of DNA polymerase α in Arabidopsis thaliana (L.) Heynh. PolA2 is a single copy gene in Arabidopsis and shows highly conserved regions with putative homologs in other plant species. Insertional inactivation of PolA2 in Arabidopsis leads to embryo lethality, with developmental arrest at or before the four-cell stage during embryogenesis. The apical cell lineage is strongly affected in the mutant embryos and the endosperm initial cell fails to divide. PolA2 is expressed broadly in the early phases of embryo development during the period of active cell divisions, while during the later stages of development expression is reduced and more localized. Ectopic overexpression of PolA2 produced dominant negative phenotypes with gametic and embryo lethality suggesting that coordinated and parallel expression with other subunits is critical for its proper function in DNA replication and plant development.

Comparative transcriptomics of seed nourishing tissues: uncovering conserved and divergent pathways in seed plants

“…One of them encompasses DEOGs involved in DNA replication (Figure 10b), encoding subunits of origin-of-replication complexes, ORC1 and ORC2 (Collinge et al, 2004;Vergara et al, 2023). Likewise, POLA2, an alpha subunit of the DNA polymerase (Yang et al, 2009), and EXO1, an exonuclease (Kazda et al, 2012), were present in this replication cluster (Figure 10b). The other cluster is composed of several DEOGs that are annotated as subunits of DNA-directed RNAPs and their accompanying proteins (Figure 10c).…”