Parental genomic imprinting in plants: Significance for reproduction

Medecine/Sciences248-9753-757MSMS

DNA methylation reprogramming during plant sexual reproduction?

10.1016/j.tig.2010.06.001Trends in Genetics269394-399TRGE

Polycomb group complexes self-regulate imprinting of the polycomb group gene MEDEA in Arabidopsis

10.1016/j.cub.2006.01.020Current Biology165486-492CUBL

Australian Cainozoic Bryozoa, 1: Nudicella gen. nov (Onychocellidae, Cheilostomata): taxonomy, palaeoenvironments and biogeography

The new bryozoan genus Nudicella (Onychocellidae, Cheilostomata) is proposed to accommodate the common and widespread Australian Cainozoic cheilostome bryozoan Eschara clarkei Tenison Woods, which is redescribed and subdivided into four species: N. clarkei (Tenison Woods), N. cribriforma sp. nov., N. latiramosa sp. nov. and N. tenuis sp. nov. Cellaria gigantea Maplestone is also reassigned to Nudicella. Colonies of this genus display a wide variety of growth forms, including cribrate fenestrate, flat robust branching, foliose, delicate branching and encrusting; their occurrences correlate with changes in sedimentary facies and palaeoenvironments. The distinctive cribrate style of fenestrate growth form has evolved convergently in unrelated bryozoan groups at various geological intervals. It is found in a wide variety of sedimentary facies, as in other coexisting opportunistic genera such as Celleporaria, indicating a wide ecological tolerance. The oldest recorded occurrence of Nudicella is in the Paleocene of north western Australia. From there it appears to spread south in the Eocene and then east towards the Otway Basin in southeastern Australia, where it occurs in the Oligocene and Miocene; no post-Miocene representatives of this genus are yet known. © 2004 Association of Australasian Palaeontologists

First fossil finds of some Australian Bryozoa (Cheilostomata)

The abundant fossil record of well-preserved Bryozoa in samples from the Tertiary of Victoria and South Australia includes some \u27first fossil finds\u27 which are recorded here. Several are of species known from the Recent of the Australian or Indo-West-Pacific regions, but some represent genera with a much wider temporal and geographical range. Of the 11 species illustrated, six are known, or may be inferred, to have inhabited \u27sand fauna\u27 environments. Specimens of one species are complete enough to allow its formal description as Chlidoniopsis inopina sp. nov. <br /

The Female Gametophyte

The angiosperm female gametophyte is critical for plant reproduction. It contains the egg cell and central cell that become fertilized and give rise to the embryo and endosperm of the seed, respectively. Female gametophyte development begins early in ovule development with the formation of a diploid megaspore mother cell that undergoes meiosis. One resulting haploid megaspore then develops into the female gametophyte. Genetic and epigenetic processes mediate specification of megaspore mother cell identity and limit megaspore mother cell formation to a single cell per ovule. Auxin gradients influence female gametophyte polarity and a battery of transcription factors mediate female gametophyte cell specification and differentiation. The mature female gametophyte secretes peptides that guide the pollen tube to the embryo sac and contains protein complexes that prevent seed development before fertilization. Post-fertilization, the female gametophyte influences seed development through maternal-effect genes and by regulating parental contributions. Female gametophytes can form by an asexual process called gametophytic apomixis, which involves formation of a diploid female gametophyte and fertilization-independent development of the egg into the embryo. These functions collectively underscore the important role of the female gametophyte in seed and food production