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K L Kelleher

Publications and source records attributed to K L Kelleher.

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Developmental expression of messenger RNA levels of the alpha subunit of the GTP-binding protein, Gz, in the mouse nervous system.

There has been recent evidence that Gz may play a role in the transmission of the neurotrophic signal from nerve terminals to the cell bodies [Johanson, S.O., Crouch, M.F., Hendry, I.A., Signal transduction from membrane to nucleus: the special case for neurons, Neurochem. Res. 21 (1996) 779-785]. We examined the developmental expression of the alpha subunit of Gz (Gzalpha) in the peripheral and central nervous systems of the mouse. Our laboratory has developed a quantitative reverse transcription-polymerase chain reaction (RT-PCR) for Gzalpha which makes use of a fragment of the PCR product shortened by 107 base pairs creating a standard which mimics the original RNA. Serial dilutions of the mouse RNA with a constant concentration of mimic RNA were made and the point where equal amounts of product are formed allows accurate measurement of Gzalpha mRNA in the tissue. We have demonstrated that in the developing mouse superior cervical ganglion (SCG), dorsal root ganglion (DRG) and trigeminal ganglion the expression of Gzalpha mRNA is highest perinatally. From 3 weeks of age, in all tissues with the exception of the SCG, Gzalpha mRNA levels fall to lower levels in the adult animal. The developmental pattern of expression of Gzalpha in both the cerebellum and the brain differs from the peripheral nervous system. In the cerebellum, Gzalpha mRNA expression is highest around birth and in the brain it is highest around third postnatal week and then the levels decline as adulthood is approached. These results suggest that the highest level of Gzalpha mRNA is expressed at the time when target tissue innervation is occurring. This further strengthens the hypothesis that Gzalpha is important in the transfer of information from target tissues to the innervating nerve cells.

Animals

Sequence similarity of phospholipase C with the non-catalytic region of src.

The production of the second messenger molecules diacylglycerol and inositol 1,4,5-trisphosphate is mediated by activated phosphatidylinositol-specific phospholipase C (PLC) enzymes. Here we report the cloning of a bovine brain complementary DNA encoding an enzyme PLC-148 that is characterized by calcium-dependent and phosphatidylinositol-specific phospholipase C activity when expressed in mammalian cells. Bovine brain messenger RNA contains a 7.5-kilobase transcript corresponding to the isolated cDNA; a related transcript of the same size is present in mRNA from some but not all human cell lines tested. Southern blot analysis of the bovine genome indicated that one or possibly two genes hybridize to the cloned PLC-148 cDNA. There is a striking sequence similarity between specific regions of PLC-148 and the non-catalytic domain of the non-receptor tyrosine kinases. The newly characterized crk transforming gene of the avian sarcoma virus CT10 also contains extensive sequence similarities with PLC-148.

Amino Acid Sequence

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Attitude to Death