LBR (lamin B receptor) is an integral protein of the inner nuclear membrane encoded by a gene on human chromosome 1q42.1. LBR has a nucleoplasmic, amino-terminal domain of approximately 200 amino acids followed by a carboxyl-terminal domain similar in sequence to yeast and plant sterol reductases. We have determined the primary structures of two human proteins with strong sequence similarity to the carboxyl-terminal domain of LBR and sterol reductases. Their genes have recently been assigned the symbols TM7SF2 and DHCR7. TM7SF2 mRNA is most predominantly expressed in heart and DHCR7 mRNA mostly in liver and brain. Whereas LBR is localized to the inner nuclear membrane, these two related proteins are in the endoplasmic reticulum. The TM7SF2 gene contains 10 coding exons, and its intron positions are exactly conserved in the part of the LBR gene encoding its carboxyl-terminal domain. Intron positions in the DHCR7 gene are also similar. Both of these new LBR-like genes are on chromosome 11q13. These results describe a human gene family encoding proteins of the inner nuclear membrane and endoplasmic reticulum that function in nuclear organization and/or sterol metabolism.

The first partially articulated scleritome of a tommotiid, Eccentrotheca sp., is described from the Lower Cambrian of South Australia. The Eccentrotheca scleritome consists of individual sclerites fused in a spiral arrangement, forming a tapering tube-shaped skeleton with an inclined apical aperture and a circular to subcircular cross section. Traditionally, tommotiid sclerites have been assumed to form a dorsal armor of imbricating phosphatic plates in slug-like bilaterians, analogous to the calcareous sclerites of halkieriids. The structure of the Eccentrotheca scleritome is here reinterpreted as a tube composed of independent, irregularly shaped sclerites growing by basal-marginal accretion that were successively fused to form a rigid, protective tubular structure. The asymmetrical shape and sometimes acute inclination of the apical aperture suggests that the apical part of the scleritome was cemented to a hard surface via a basal disc, from which it projected vertically. Rather than being a vagrant member of the benthos, Eccentrotheca most likely represented a sessile, vermiform filter feeder. The new data suggest that the affinities of Eccentrotheca, and possibly some other problematic tommotiids, lie with the lophophorates (i.e., the phoronids and brachiopods), a clade that also possesses a phosphatic shell chemistry and a sessile life habit.4 page(s

The tannuolinidMicrinabelongs to the tommotiids—a common and widely distributed, but poorly understood, group of Early Cambrian fossil metazoans with multiple external organophosphatic sclerites. Recent findings of sessile articulated tommotiid scleritomes indicate that previous reconstructions of tommotiids as slug-like bilaterians with a dorsal cover of sclerites require detailed re-evaluation. Comparative ultrastructural work has already indicated that the tommotiids might be a sister group to the Brachiopoda, withMicrinarepresenting the most derived and brachiopod-like bimembrate tommotiid. Here we further develop and strengthen this controversial phylogenetic model with a new reconstruction ofMicrina, where the two types of sclerites—mitral and sellate—belong to a near bilaterally symmetrical bivalved sessile organism. This new scleritome configuration was tested by recreating an articulated bivalvedMicrinafrom isolated mitral and sellate sclerites; both sclerites have muscles that would have enabled movement of the sclerites. The mitral and sellate sclerites ofMicrinaare considered to be homologous with the ventral and dorsal valves, respectively, of organophosphatic linguliform brachiopods, indicating that a simple type of filter-feeding within an enclosed bivalved shell had started to evolve in derived tannuolinids. The new reconstruction also indicates that the phylogenetic range of ‘bivalved’, sessile lophophorates is larger than previously suspected.