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K Brasch

Publications and source records attributed to K Brasch.

28 records · Page 2Linked to original sources

The organization, composition and matrix of hepatocyte nuclei exposed to alpha-amanitin.

Alterations in the structure and molecular composition of avian hepatocyte nuclei were compared following administration in vivo of lethal and sub-lethal doses of alpha-amanitin. This toxin interferes with extranucleolar transcription by direct inhibition of RNA polymerase II activity. the resultant effects include: extensive condensation of chromatin, displacement of nucleoplasmic contents and fragmentation of nucleoli. Changes in nuclear morphology were quantitated by stereometry and related to variations in RNA and residual, non-histone proteins (NHP). Gross alterations in nuclear structure and depletion of RNA and NHP levels were of similar magnitude with both doses of amanitin. The effects were fully reversible, however, with a minimal dose but terminal with a lethal dose. DNA and histone protein levels remained unchanged at all stages. These results imply that the process of transciption may itself keep and/or maintain chromatin in a dispersed state, and that in the absence of transcription chromatin naturally condenses. Modification of nuclear proteins may be necessary only to maintain chromatin compacted permanently or for extended periods of time. A model of nuclear organization is proposed to incorporate these considerations and to identify the probable location of the nuclear matrix in situ.

Amanitins↗

The morphology of erythroid cells separated by density gradient centrifugation through Ficoll.

The regenerating blood of geese injected with phenylhydrazine was subjected to large scale, zonal centrifugation through density gradients of Ficoll. In this way, erythroid cells were fractionated according to their respective stages of development. Highly enriched fractions were obtained, containing cells that were well preserved as assessed by both light and electron microscopy. The separated cells exhibited ribosome density and nucleic acid and protein staining patterns typically associated with erythrocyte differentiation. Morphometric analysis of nuclei indicated that despite an apparent net increase in the amount of compact chromatin during development, comparatively little difference existed between the volumes of condensed chromatin present in immature and mature cells. Instead, there was a three fold decrease in nuclear volume between young erythroblasts and reticulocytes, coupled with a concomitant decrease in the volume occupied by dispersed chromatin, RNP and nucleoli. These observations are discussed in relation to molecular changes associated with nuclear differentiation in erythroid cells.

Animals↗

The nucleated erythrocyte: a model of cell differentiation.

The process of erythropoiesis is characterized by several distinctive features which render it a very useful model of cell differentiation. Mature erythrocytes arise from stem cells in a series of intermediate stages which are fairly well defined both on morphological and on biochemical grounds. During this development, the erythrocytes genome is gradually inactivated and the cell becomes geared to the production of primarily one gene product, hemoglobin. Recently, erythropoiesis has been closely studied in avian species since it has become technically possible to fractionate the blood of anemic birds into high-yield populations of young, developing and mature red cells. Attention has focused on patterns of RNA synthesis including globin m-RNA, in relation to cytoplasmic constitutents becoming modified for reduced activity. From the point of view of gene regulation, erythrocyte development is especially interesting in non-mammals, where in contrast to mammals, even fully mature red cells retain their nuclei. These erythrocytes rank among the most extreme examples of cell specialization and gene repression known. The nuclei of avian erythrocytes and others, contain a tissue-specific histone protein in addition to the more usual complement of vertebrate histone. This histone (H5, V, F2c) has been extensively investigated with a view to linking its presence to structural and molecular changes involved in the condensation and repression of red cell nuclei. The evidence to dat suggests that H5, in conjunction with tissue-specific changes in non-histone proteins, may be responsible for keeping the genomes of nucleated erythrocytes permanently inactive.

Animals↗

Assignment of multiple endocrine neoplasia type 2A to chromosome 10 by linkage.

Multiple endocrine neoplasis type 2A (MEN2A) is one of several kinds of cancers that appear to be inherited in an autosomally dominant fashion. We have assigned the MEN2A locus to chromosome 10 by linkage with a new DNA marker (D10S5). The linkage led us to investigate other chromosome 10 markers and demonstrate linkage between the disease locus and the interstitial retinol-binding protein (IRBP) gene. The D10S5 locus was sublocalized to 10q21.1 by hybridization in situ and the IRBP gene to p11.2----q11.2 with a secondary site at q24----q25. The linkages were established using 292 members of five families, three different restriction fragment length polymorphisms (RFLPs) at D10S5 and two RFLPs recognized by the IRBP probe. The recombination frequencies from pairwise linkage analysis between the disease and two marker loci D10S5 and IRBP were 0.19 and 0.11, with maximum lod scores of 3.6 and 8.0 respectively. Ordering of the three loci by multipoint analysis placed the IRBP gene approximately midway between the disease and D10S5 loci.

Chromosome Mapping↗