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Clathrin light chain B: Gene structure and neuron-specific splicing

  • Stefan Stamm
  • , Diana Casper
  • , Jonathan Dinsmore
  • , Charles A. Kaufmann
  • , Jürgen Brosius
  • , David M. Helfman

Producción científica: Articlerevisión exhaustiva

39 Citas (Scopus)

Resumen

The clathrin light chains are components of clathrin coated vesicles, structural constituents involved in endocytosls and membrane recycling. The clathrin light chain B (LCB) gene encodes two isoforms, termed LCB2 and LCB3, via an alternative RNA splicing mechanism. We have determined the structure of the rat clathrin light chain B gene. The gene consists of six exons that extend over 11.9 kb. The first four exons and the last exon are common to the LCB2 and LCB3 isoforms. The fifth exon, termed EN, is included in the mRNA in brain, giving rise to the brain specific form LCB2 but is excluded in other tissues, generating the LCB3 isoform. Primary rat neuronal cell cultures express predominantly the brain specific LCB2 isoform, whereas primary rat cultures of glia express only the LCB3 isoform, suggesting that expression of the brain-specific LCB2 form is limited to neurons. Further evidence for neuronal localization of the LCB2 form is provided using a teratocarcinoma cell line, P19, which can be induced by retinoic acid to express a neuronal phenotype, concomitant with the induction of the LCB2 form. In order to determine the sequences involved in alternative splice site selection, we constructed a minigene containing the alternative spliced exon EN and its flanking intron and exon sequences. This minigene reflects the splicing pattern of the endogenous gene upon transfection in HeLa cell and primary neuronal cell cultures, indicating that this region of the LCB gene contains all the necessary information for neuron-specific splicing.

Idioma originalEnglish
Páginas (desde-hasta)5097-5103
Número de páginas7
PublicaciónNucleic Acids Research
Volumen20
N.º19
DOI
EstadoPublished - oct 11 1992

Nota bibliográfica

Funding Information:
We thank R.Hynes for the XEMBL3B rat liver library. JD wants to thank M.McBurney and M.Rudnicki for providing P19 embryonal carcinoma cells. We thank H.Nawa for primary cortex, SCG and glial cultures. pTKB2 and pTKB3 were a generous gift from T.Kirchhausen. J.D. was supported by a postdoctoral fellowship from the American Cancer Society and by a National Cancer Institute grant to F.Solomon (MIT). C.A.K. is supported by a Physician Scientist Award NIMH Kll-MH 00682. S.S. is supported by a fellowship of the Gottlieb Daimler-and Karl Benz-Stiftung # 2.88.9. J.B. is supported by a grant from NIMH MH38819. D.M.H. is supported by a National Institutes of Health Grant R01-GM43040 and is an Established Investigator of the American Heart Association.

Financiación

We thank R.Hynes for the XEMBL3B rat liver library. JD wants to thank M.McBurney and M.Rudnicki for providing P19 embryonal carcinoma cells. We thank H.Nawa for primary cortex, SCG and glial cultures. pTKB2 and pTKB3 were a generous gift from T.Kirchhausen. J.D. was supported by a postdoctoral fellowship from the American Cancer Society and by a National Cancer Institute grant to F.Solomon (MIT). C.A.K. is supported by a Physician Scientist Award NIMH Kll-MH 00682. S.S. is supported by a fellowship of the Gottlieb Daimler-and Karl Benz-Stiftung # 2.88.9. J.B. is supported by a grant from NIMH MH38819. D.M.H. is supported by a National Institutes of Health Grant R01-GM43040 and is an Established Investigator of the American Heart Association.

FinanciadoresNúmero del financiador
National Institutes of Health (NIH)R01-GM43040
National Institutes of Health (NIH)
National Institute of Mental HealthR01MH038819, Kll-MH 00682
National Institute of Mental Health
American Cancer Society-Michigan Cancer Research Fund
National Childhood Cancer Registry – National Cancer Institute
American the American Heart Association
Massachusetts Institute of Technology

    ASJC Scopus subject areas

    • Genetics

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