Integrins are heterodimeric transmembrane receptors that modulate cell adhesion, migration, and signaling. Multiple integrin chains contribute to development and morphogenesis of a given tissue. Here, we analyze the expression of Drosophila integrin alpha chains in the ovarian follicular epithelium, a model for tissue morphogenesis and cell migration. We find expression throughout development of the beta chain, ␤PS. Alpha chains, however, exhibit both spatial and temporal expression differences. ␣PS1 and ␣PS2 integrins are detected during early and mid-oogenesis on apical, lateral, and basal membranes with the ␤PS chain, whereas ␣PS3-family integrins (␣PS3, ␣PS4, ␣PS5) are expressed in anterior cells late in oogenesis. Surprisingly, we find that ␣PS3-family integrins are dispensable for dorsal appendage morphogenesis but play a role in the final length of the egg, suggesting redundant functions of integrins in a simple tissue. We also demonstrate roles for ␣PS3␤PS integrin in border cell migration and in stretch cells. Developmental Dynamics 237:3927-3939, 2008.

The thyroid hormone receptor ␣1 (TR␣) exhibits a dual role as an activator or repressor of its target genes in response to thyroid hormone (T 3 ). Previously, we have shown that TR␣, formerly thought to reside solely in the nucleus bound to DNA, actually shuttles rapidly between the nucleus and cytoplasm. An important aspect of the shuttling activity of TR␣ is its ability to exit the nucleus through the nuclear pore complex. TR␣ export is not sensitive to treatment with the CRM1-specific inhibitor leptomycin B (LMB) in heterokaryon assays, suggesting a role for an export receptor other than CRM1. Here, we have used a combined approach of in vivo fluorescence recovery after photobleaching experiments, in vitro permeabilized cell nuclear export assays, and glutathione S-transferase pull-down assays to investigate the export pathway used by TR␣. We show that, in addition to shuttling in heterokaryons, TR␣ shuttles rapidly in an unfused monokaryon system as well. Furthermore, our data show that TR␣ directly interacts with calreticulin, and point to the intriguing possibility that TR␣ follows a cooperative export pathway in which both calreticulin and CRM1 play a role in facilitating efficient translocation of TR␣ from the nucleus to cytoplasm. The thyroid hormone receptor ␣1 (TR␣)4 is a member of the nuclear receptor superfamily of transcription factors. TR␣ acts as an intracellular receptor for thyroid hormone (T 3 ), thereby regulating expression of T 3 -responsive genes associated with many aspects of development, growth, and metabolism. Among the nuclear receptors, TR␣ is particularly intriguing in that it can modulate transcription whether or not it is bound to T 3 . Consistent with this dual role as an activator or repressor of transcription, at steady state TR␣ appears to be almost exclusively localized in the nucleus. However, we have shown that the receptor, in fact, shuttles rapidly between the nucleus and cytoplasm (1). Whereas the significance of this nucleocytoplasmic shuttling remains to be precisely characterized, this activity may be related directly to regulation of TR␣ target genes as well as to yet unknown non-genomic functions (2).Nucleocytoplasmic shuttling occurs as a result of a dynamic balance between the recognition of nuclear localization signals (NLS) and nuclear export signals (NES) by particular import and export factors termed importins and exportins, respectively (3). Most nuclear receptors appear to enter the nucleus via importin ␣/␤ recognition and subsequent translocation through the nuclear pore complex (3, 4). Unlike nuclear import, however, the export pathways followed by nuclear receptors remain more elusive.The most thoroughly studied and well characterized nuclear export pathway involves the exportin CRM1. Many shuttling transcription factors outside of the nuclear receptor superfamily follow a CRM1-dependent mechanism (5, 6). Like other nuclear receptors, however, TR␣ lacks the leucine-rich NES associated with classical CRM1-mediated nuclear export (1, 7). Concordantly, we ha...