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Biochem Biophys Res Commun ; 194(1): 552-9, 1993 Jul 15.
Article in English | MEDLINE | ID: mdl-7687439

ABSTRACT

cDNA clones encoding the low molecular weight GTP-binding proteins ral A (951 bp) and ral B (2073 bp), including the entire coding region (618 bp), were isolated from a rat PC12 pheochromocytoma library. Northern analyses demonstrated that both ral A and ral B are widely expressed in rat tissues. Two ral A transcripts of 1.1 and 2.9 kb were observed in most tissues in varying proportions. The 1.1 kb ral A band of testes was further shown to be composed of two closely migrating species. In contrast to these findings, a single ral B transcript of 2.3 kb was detected in most tissues. Steady-state levels of ral A transcripts appear greater than ral B. Quantitatively, the testes exhibited the highest ral A and ral B mRNA levels, with lower levels observed in the brain, adrenal and pituitary glands, kidney and ovary. Ral mRNA levels were lowest in muscle tissue, particularly skeletal muscle.


Subject(s)
GTP-Binding Proteins/biosynthesis , GTP-Binding Proteins/genetics , Gene Expression , Amino Acid Sequence , Animals , Base Sequence , Blotting, Northern , Cloning, Molecular , DNA/isolation & purification , Gene Library , Humans , Molecular Sequence Data , PC12 Cells , Poly A/genetics , Poly A/isolation & purification , Polymerase Chain Reaction , RNA/genetics , RNA/isolation & purification , RNA, Messenger/isolation & purification , RNA, Messenger/metabolism , Rats , Restriction Mapping , Sequence Homology, Amino Acid , Transcription, Genetic , ral GTP-Binding Proteins
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