Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Comparative Study
. 1995 Jul;20(7):833-46.
doi: 10.1007/BF00969696.

Expression of low-molecular-weight neurofilament (NF-L) mRNA during postnatal development of the mouse brain

Affiliations
Comparative Study

Expression of low-molecular-weight neurofilament (NF-L) mRNA during postnatal development of the mouse brain

R Kure et al. Neurochem Res. 1995 Jul.

Abstract

A regional Northern blot analysis demonstrated that the highest levels of NF-L mRNA in the adult mouse brain are present in brain stem followed by mid-brain, with lower levels found in neocortex, cerebellum, and hippocampus. The study was extended to the cellular level over course of postnatal development using in situ hybridization. This developmental analysis revealed that the expression of NF-L mRNA closely follows the differentiation pattern of many large neurons during postnatal neurogenesis. Neurons which differentiate early such as Purkinje, mitral, pyramidal, and large neurons of brain stem and thalamic nuclei, expressed high levels of NF-L mRNA at postnatal day 1. Early expression of NF-L mRNA may be required for the maintenance of the extensive neurofilament protein networks that are detected within the axons of larger neurons. Smaller neurons which differentiate later, such as dentate gyrus granule cells, small pyramidal and granule cells of the neocortex, and granule cells of the cerebellum, exhibit a delayed expression of NF-L mRNA.

PubMed Disclaimer

Similar articles

Cited by

References

    1. Cell. 1993 Apr 9;73(1):23-33 - PubMed
    1. J Biol Chem. 1990 Nov 15;265(32):19786-91 - PubMed
    1. J Cell Biol. 1975 Aug;66(2):351-66 - PubMed
    1. Proc Natl Acad Sci U S A. 1987 May;84(10):3472-6 - PubMed
    1. J Neurosci. 1990 Mar;10(3):764-84 - PubMed

Publication types

MeSH terms

LinkOut - more resources