Charles Daniel Lane

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For the American mine owner, see Charles D. Lane.
Charles Daniel Lane
Photo Charles Lane.jpg
Born
London, England
CitizenshipBritish
EducationTrinity College, Cambridge, Christ Church, Oxford, The Zoology Department, Oxford, The Laboratory of Molecular Biology, Cambridge (UTC) The National Institute for Medical Research (Mill Hill, London UTC)
OccupationMolecular biologist

Charles Daniel Lane is a British molecular biologist who along with colleagues Gerard Marbaix and John Gurdon discovered the oocyte exogenous mRNA expression system – a system that not only reveals aspects of the control of gene expression but also provides a "living test tube" for the study of macromolecules: such an whole cell system also shows the merits of a non-reductionist approach, and the possibility of mRNA therapeutics.

Early life and education[]

As a boy, Charles displayed a passion for moths, butterflies and plants and with the aid of his mother (Miriam Lane, a biologist and nature conservationist), wrote a number of "anecdotal" papers on subjects such as the migration of butterflies. Charles was also a significant collector of Meadow Brown butterflies for the population genetic studies of E.B. Ford.

Leaving school at 16, Lane joined the biochemistry laboratory of Hans Krebs: much of Lane's work involved studying pyruvate kinase in slices and in homogenates of rat liver. Lane attended Trinity College, Cambridge and Christ Church, Oxford. His University of Oxford doctoral thesis was "The Microinjection of RNA into Eggs and Oocytes of Xenopus Laevis".[1] A hard copy of the thesis can be viewed at the Bodleian Library, Oxford. He then worked at the Medical Research Council Molecular Biology Laboratories at Cambridge and then at the National Institute for Medical Research, at Mill Hill London.

Career and research[]

Lane is known for the discovery (with colleagues Gerard Marbaix and John Gurdon), of the oocyte surrogate gene expression system, and its subsequent development and refinement (with many colleagues for the study of post translational events including the study of proteins embedded in cell membranes. Lane believed that John Gurdon’s studies on gene expression enjoyed further potential.

The discovery that living cells programmed with exogenous messenger RNA can make and correctly modify foreign proteins is, for three separate reasons, arguably one of the most important scientific advances of the last 50 years. Thus:

  • The foreign mRNA can reveal control mechanisms within the living cell.
  • Foreign proteins made within a living cell provide a “living test tube” for the discovery and study of molecules, including many pharmaceuticals – such as those that interact with receptor proteins embedded in cell membranes.
  • Messenger RNA Therapeutics may revolutionize many conventional medical treatments – from anti-viral vaccines to heart medicines to cancer vaccines.  However, to date no mRNA Therapeutic has yet reached the market place (including COVID-19 Vaccines).

The first key experiment was performed in 1968 by Lane and John Gurdon followed by a second key experiment involving Gerard Marbaix.,[2] verified afterwards:[3] the general characteristics of the novel mRNA expression experimental system were then defined [4]

A vital question was the extent to which the living oocyte could carry out post-translational modifications and the answer, indicating near universality, began to emerge[5] &.[6]  The ability of the oocyte to process correctly and locate correctly foreign particles renders this whole cell system generally useful. The system has also been used to evaluate control systems within the living cell. This basic discovery has generated a significant literature and the Xenopus oocyte microinjection system has become a standard feature of many laboratories, whilst the philosophy behind using the cell as a “living test tube” has spread far beyond the simple oocyte system – not least to mRNA therapeutics.

In 1976 Scientific American published [6] a popular article by Lane entitled "Rabbit Haemoglobin from Frog Eggs".

The initial studies which led to this discovery, were performed in the old Zoology Department building (at Oxford). Even before Lane had finished his doctoral thesis he was elected (age 22) a Research Fellow of Trinity College, Cambridge – one of the youngest persons ever to be elected a Fellow of a Cambridge College.[citation needed]

Lane had realized that the oocyte system enjoyed enormous potential for the study of post translational events, and an early (1971) Proceeding of the National Academy of Sciences paper with Hans Bloemendal, Anton Berns, Ger Strous and Michael Matthews focused on that which, in terms of post-translational events, the oocyte system could and could not do,. Thing it could not do turned out to be extremely rare – the oocyte could even accurately modify honey bee promelittin made under the direction of injected venom gland mRNA [7] and could even, insert foreign proteins into membranes in a functional state.[8]  For about 14 years, Lane's research focused on the oocyte as a system for studying post translational (and other) downstream events. Lane was not interested in the use of the oocyte as a system for studies with exogenous DNA, believing that other systems were better suited to upstream studies: nonetheless, the oocyte system has its uses for such endeavours, especially as regards the study of transcription.

References & publications[]

  1. ^ "Copy of Thesis". www.ohllimited.co.uk. Retrieved 2020-11-04.
  2. ^ Lane, C. D.; Marbaix, G.; Gurdon, J. B. (1971-10-14). "Rabbit haemoglobin synthesis in frog cells: the translation of reticulocyte 9 s RNA in frog oocytes". Journal of Molecular Biology. 61 (1): 73–91. doi:10.1016/0022-2836(71)90207-5. ISSN 0022-2836. PMID 5169490.
  3. ^ Marbaix, G.; Lane, C. D. (1972-06-28). "Rabbit haemoglobin synthesis in frog cells: II. Further characterization of the products of translation of reticulocyte 9 s RNA". Journal of Molecular Biology. 67 (3): 517–524. doi:10.1016/0022-2836(72)90469-X. ISSN 0022-2836. PMID 5065205.
  4. ^ Gurdon, J. B.; Lane, C. D.; Woodland, H. R.; Marbaix, G. (1971). "Use of Frog Eggs and Oocytes for the Study of Messenger RNA and its Translation in Living Cells". Nature. 233 (5316): 177–182. Bibcode:1971Natur.233..177G. doi:10.1038/233177a0. ISSN 1476-4687. PMID 4939175. S2CID 4160808.
  5. ^ Berns, A. J. M.; Kraaikamp, M. Van; Bloemendal, H.; Lane, C. D. (1972). "Calf Crystallin Synthesis in Frog Cells: The Translation of Lens-Cell 14S RNA in Oocytes". Proceedings of the National Academy of Sciences of the United States of America. 69 (6): 1606–1609. Bibcode:1972PNAS...69.1606B. doi:10.1073/pnas.69.6.1606. ISSN 0027-8424. PMC 426758. PMID 4504377.
  6. ^ Jump up to: a b Lane, C. (1976). "Rabbit hemoglobin from frog eggs". Scientific American. 235 (2): 61–69, 71. Bibcode:1976SciAm.235b..60L. doi:10.1038/scientificamerican0876-60. ISSN 0036-8733. PMID 945908.
  7. ^ Kindås-Mügge, Ingela; Lane, C. D.; Kreil, G. (1974-08-15). "Insect protein synthesis in frog cells: The translation of honey bee promelittin messenger RNA in Xenopus oocytes". Journal of Molecular Biology. 87 (3): 451–462. doi:10.1016/0022-2836(74)90096-5. ISSN 0022-2836. PMID 4444031.
  8. ^ Ohlsson, R. I.; Lane, C. D.; Guengerich, F. P. (1981). "Synthesis and insertion, both in vivo and in vitro, of rat-liver cytochrome P-450 and epoxide hydratase into Xenopus laevis membranes". European Journal of Biochemistry. 115 (2): 367–373. doi:10.1111/j.1432-1033.1981.tb05247.x. ISSN 0014-2956. PMID 6165584.

Further works & reviews[]

  • Lane CD, Marbaix G and Gurdon JB (1971) 9S RNA from reticulocytes and is assay in frog oocytes.  The Biology & Radiobiology of Anucleate Systems Academic Press.  Ed S. Bonotto
  • Lane CD, Marbaix G et Gurdon JB (1972).  Traduction du RNA 9S de reticulocytes de lapin en chaines de globine dan les oeufs et les oocytes de xenope.  Archive Internationales de Physiologie et de Biochimie 80 (5) pages 973-974
  • Lane CD, Marbaix G and Gurdon JB (1971).   The translation of reticulocyte 9S RNA in frog oocytes gives rise to alpha and beta globin chains.  Communication to FEBS meeting at Vauna, Bulgaria
  • Lane CD and Morel C (1972).  The translation of duck 9S RNA in frog oocytes.  Communication to the Biochemical Society of Brazil
  • Bloemendal H, Berns A, Strous G, Matthews M, and Lane CD (1972). Translation of eukaryotic messenger RNA in various heterologous systems. “RNA Viruses/Ribosomes” Pub. North-Holland
  • Smith M, Stavnezar J, Huang R-C, Gurdon JB and Lane CD (1973).  Mouse immunoglobin synthesis in frog cell: the translation of9-13S myeloma RNA in frog oocytes.  Journal of Molecular Biology 80 pages 553-557
  • Jacobson A, Lane CD and Alton T (1975).  Electrophoretic separation of the major species of slime mould messenger RNA. “Microbiology” (Proc. Of Asiolma Symp) Ed. Dworkin & Shapiro.
  • Jacobson A, Palatnik CM, Lane CD, Mabie C and Wilkins C (1975).  Fractionation of mRNAs from Dictyostelium discoideum EMBO workshop on Development and Differentiation in slime molds Ed. P Capucinelli North-Holland Press Amsterdam
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