𝔖 Bobbio Scriptorium
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Activation and inactivation of genes determining hemoglobin types

✍ Scribed by W. French Anderson; Jane E. Barker; Norton A. Elson; William C. Merrick; Alan W. Steggles; Golder N. Wilson; Judith A. Kantor; Arthur W. Nienhuis


Book ID
102883568
Publisher
John Wiley and Sons
Year
1975
Tongue
English
Weight
834 KB
Volume
85
Category
Article
ISSN
0021-9541

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✦ Synopsis


Globin gene switching in sheep and goats has been used as a model system for examining gene expression in differentiating red blood cells. Sheep and goats switch from the synthesis of hemoglobin A to hemoglobin C in response to erythropoietin. The regulatory mechanism producing this switch in hemoglobin types could occur at the cellular, nuclear, or cytoplasmic level. Evidence is presented which suggests that regulation is occurring, in fact, at the nuclear level. Sheep and goat erythroid colonies have been grown in plasma clot culture in order to study the synthesis of individual globin chains. Erythropoietin is required for colony formation. The switch from hemoglobin A to hemoglobin C synthesis requires not only colony formation but also a higher concentration of erythropoietin than is required just for the production of colonies. A cell-free transcriptional system using bone marrow chromatin and mammalian DNA-dependent RNA polymerase has been developed in order to examine the nuclear control mechanisms in more detail.


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## Abstract Telomerase activation, a critical event in human carcinogenesis, may result from defects in telomerase‐repressing mechanisms. Data from microcell‐mediated chromosome transfer (MMCT) suggests the presence of telomerase repressor genes that become inactivated during carcinogenic processes