Functional MRI measurements can securely partition the human posterior occipital lobe into retinotopically organized visual areas (V1, V2 and V3) with experiments that last only 30 min. Methods for identifying functional areas in the dorsal and ventral aspect of the human occipital cortex, however, have not achieved this level of precision; in fact, different laboratories have produced inconsistent reports concerning the visual areas in dorsal and ventral occipital lobe. We report four findings concerning the visual representation in dorsal regions of occipital cortex. First, cortex near area V3A contains a central field representation that is distinct from the foveal representation at the confluence of areas V1, V2 and V3. Second, adjacent to V3A there is a second visual area, V3B, which represents both the upper and lower quadrants. The central representation in V3B appears to merge with that of V3A, much as the central representations of V1/2/3 come together on the lateral margin of the posterior pole. Third, there is yet another dorsal representation of the central visual field. This representation falls in area V7, which includes a representation of both the upper and lower quadrants of the visual field. Fourth, based on visual field and spatial summation measurements, it appears that the receptive field properties of neurons in area V7 differ from those in areas V3A and V3B.

We describe the first systematic functional magnetic resonance imaging (fMRI) measurements of visual field maps in macaque visual cortex. The boundaries of visual areas V1, V2, V3, V3A, V4, MT/V5, and TEO/V4A were identified using stimuli that create traveling waves of activity in retinotopically organized areas of the visual cortex. Furthermore, these stimuli were used to measure the dimensions of the representations of the central 11 degrees in V1-V3, quantitative visual field eccentricity functions for V1-V3 and MT, and the distribution of foveal and peripheral signals within the occipital lobe. Within areas V1, V2, MT, and portions of V4, the fMRI signals were 5-10 times the noise level (3 mm3 volumes of interest). Signals were weaker but still significant in other cortical regions, including V3, V3A, and TEO. There is good agreement between the fMRI maps and the visual area maps discovered using local anatomical and physiological measurements. The fMRI measurements allow one to obtain a broad view of the distribution of cortical signals, spanning multiple visual areas at a single point in time. The combination of scale and sensitivity demonstrated here create a good foundation for measuring how localized signals and lesions influence the responses and reorganization in widely separated cortical regions. The ability to measure human and macaque maps using the same technology will make it possible to define computational homologies between the two species.

Abstract. Filaments and fibrils that exhibit a 100-nm axial periodicity and occur in the medium and in the deposited extracellular matrix of chicken embryo and human fibroblast cultures have been tentatively identified with type VI collagen on the basis of their similar structural characteristics (Bruns, R. R., 1984, J. Ultrastruct. Res.,. Using indirect immunoelectron microscopy and specific monoclonal and polyclonal antibodies, we now report their positive : identification with collagen VI and their distribution in fibroblast cultures and in tendon. Primary human foreskin fibroblast cultures, labeled with anti-type VI antibody and studied by fluorescence microscopy, showed a progressive increase in labeling and changes in distribution with time up to 8 d in culture. With immunoelectron microscopy and monoclonal antibodies to human type VI collagen followed by goat antimouse IgG coupled to colloidal gold, they showed in thin sections specific 100-nm periodic labeling on extracellular filaments and fibrils: one monoclonal antibody (3C4) attached to the band region and another (4B10) to the interband region of the filaments and fibrils. Rabbit antiserum to type VI collagen also localized on the band region, but the staining was less well defined. Control experiments with antibodies to fibronectin and to procollagen types I and IU labeled other filaments and fibrils, but not those with a 100-nm period. Heavy metal-stained fibrils with the same periodic and structural characteristics also have been found in both adult rat taft tendon and embryonic chicken tendon subjected to prolonged incubation in culture medium or treatment with adenosine 5'-triphosphate at pH 4.6. We conclude that the 100-nm periodic filaments and fibrils represent the native aggregate form of type VI collagen. It is likely that banded fibrils of the same periodicity and appearance, reported by many observers over the years in a wide range of normal and pathological tissues, are at least in part, type VI collagen. WITH the discovery of the genetic heterogeneity of collagen (38), it became apparent that the composition and organization of the extracellular matrices were far more complex than were ever anticipated. To date there are at least 10 known, distinct collagen gene products, not including non-matrix collagen sequences such as those in Clq (47, 48), acetylcholine esterase (50), and surfactant (60). The molecular structure and tissue supramolecular aggregates of most of these are established. For several, however, the forms in which they exist in situ and their relations with other matrix components are not yet known. Type VI collagen is an example of the latter.Extracellular filaments and fibrils that have a 100-nm periodic cross-banding have been observed in chicken embryo fibroblast cultures (7). The basic unit, a "beaded" filament, consists of a thread measuring 2-3 nm in diameter and pairs of "beads" distributed along its length at regular intervals of 90-110 nm. In the aggregated form (i.e., bundles of ordered "beaded" filaments), the...

Animal cloning can be achieved through somatic cell nuclear transfer (SCNT), although the live birth rate is relatively low. Recent studies have identified H3K9me3 in donor cells and abnormal Xist activation as epigenetic barriers that impede SCNT. Here we overcome these barriers using a combination of Xist knockout donor cells and overexpression of Kdm4 to achieve more than 20% efficiency of mouse SCNT. However, post-implantation defects and abnormal placentas were still observed, indicating that additional epigenetic barriers impede SCNT cloning. Comparative DNA methylome analysis of IVF and SCNT blastocysts identified abnormally methylated regions in SCNT embryos despite successful global reprogramming of the methylome. Strikingly, allelic transcriptomic and ChIP-seq analyses of pre-implantation SCNT embryos revealed complete loss of H3K27me3 imprinting, which may account for the postnatal developmental defects observed in SCNT embryos. Together, these results provide an efficient method for mouse cloning while paving the way for further improving SCNT efficiency.