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E BELL

Publications and source records attributed to E BELL.

At least 19 recordsLinked to original sources

MESSENGER RNA UTILIZATION DURING DEVELOPMENT OF CHICK EMBRYO LENS.

A marked increase in synthesis or availability of messenger RNA which can accommodate eight to ten ribosomes was observed in the chick embryo lens between 11 and 12 days of development. The increase is seen in a shift from polyribosomes consisting of predominantly two to five single ribosomes to polyribosomes of predominantly eight to ten ribosomes in lens cells. Short-lived (half-life, 3 hours) and long-lived (half-life, 30 hours) messenger RNA's coexist in whole lenses on the 14th day of development.

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PROTEIN SYNTHESIS DURING DEVELOPMENT: CONTROL THROUGH MESSENGER RNA.

Utilization of long-lived messenger RNA appears to be the exception rather than the rule in cells which are differentiating and synthesizing large amounts of specialized product at the same time. The fact that polyribosomes synthesize protein after RNA synthesis is turned off by actinomycin D is used to demonstrate messenger RNA of long half-life. The data suggest that most tissues examined have short-lived messenger RNA's, but the ocular lens can synthesize protein after an incubation of 24 hours in 40 microg of actinomycin D per milliliter. A common basis for the presence of long-lived messenger RNA in the cells of the lens, the feather, and in reticulocytes is discussed.

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RIBOSOMAL RNA IN THE DEVELOPING CHICK EMBRYO.

Developing chick embryos from the stage of primitive-streak formation make ribosomal (28S and 16S) RNA. The size and composition of the RNA appears to be constant throughout the first 7 days of development.

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Development of feather keratin during embryogenesis of the chick.

The development of keratin in 9 to 17 day embryonic chick feathers has been studied by x-ray diffraction and cytochemical methods. The x-ray diffraction pattern given by the 9-day feathers contains none of the features seen in the adult pattern. In the 10 to 11 day patterns, besides two diffuse rings centered at 4.7 A and 10 A, two sharp, rather weak rings are seen at 35 A and 4.2 A with slight preferred orientations about the equator and the meridian, respectively. At 12 days, in addition to the foregoing, a sharp intense equatorial reflection at approximately 56 A is observed. On treatment with lipid solvents, the 35 A ring is removed; prolonged extraction removes the 4.2 A ring, while blurring the 56 A reflection and enhancing the central low angle scatter. The 14-day pattern shows, besides all the features seen in the earlier patterns, a 23 A meridional reflection and other meridional and near meridional reflections. All the basic features of the adult pattern are seen at this stage and remain essentially intact on lipid extraction. Beyond 14 days, the pattern remains essentially the same, only improving in clarity and detail. The 4.2 A ring seen in the 10 to 15 day pattern is scarcely detectable in the 16-day pattern. Cytochemical evidence indicates that extensive -S-S bond formation occurs between the 13th and 14th days. It is suggested that lipids serve as a framework for the developing keratin structure which acquires permanent stability through hydrogen bonds and disulfide cross-links. The relation between keratin synthesis and tissue architecture as well as cytodifferentiation is discussed.

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