Submitted Successfully!
Thank you for your contribution! You can also upload a video entry related to this topic through the link below:
https://encyclopedia.pub/user/video_add?id=5151
Check Note
2000/2000
Ver. Summary Created by Modification Content Size Created at Operation
1 + 590 word(s) 590 2020-12-15 07:47:57
CLN3 Gene

CLN3, battenin

  • genes

1. Normal Function

The CLN3 gene provides instructions for making a protein that is found in tissues throughout the body, yet its function is unclear. The CLN3 protein is found in many compartments within cells, but its role in lysosomes is most well-studied. Lysosomes are cellular compartments that digest and recycle different types of molecules. The CLN3 protein spans the membrane surrounding lysosomes, helping to facilitate communication between it and the rest of the cell.

Studies have associated the CLN3 protein with many cellular processes, including recycling of worn-out cell parts and unneeded proteins (autophagy), maintenance of the relative acidity (pH) of lysosomes, the movement of molecules from the cell surface into the cell (endocytosis), transportation (trafficking) of proteins to where they are needed in the cell, self-destruction of cells (apoptosis), cell growth and division (proliferation), and maintenance of the body's water balance (osmoregulation). It is uncertain which of these varied functions is the primary role of the CLN3 protein, or if these processes instead represent downstream effects.

2. Health Conditions Related to Genetic Changes

2.1. CLN3 Disease

More than 65 mutations in the CLN3 gene have been found to cause CLN3 disease. CLN3 disease is an inherited disorder that begins in childhood and primarily affects the nervous system. People with this condition develop worsening vision impairment, intellectual disability, movement problems, speech difficulties, and seizures.

One CLN3 gene mutation, found in the vast majority of cases, deletes about 1,000 DNA building blocks (base pairs) in the gene. This mutation, which is usually called the 1 kilobase (kb) deletion, often occurs in both copies of the CLN3 gene. The 1 kb deletion removes a piece of the CLN3 gene and leads to the production of an abnormally short protein. As a result, the abnormal CLN3 protein is broken down or may interfere with normal cellular processes. Other mutations reduce the amount of normal protein or impair its function. It is not known how loss of this protein causes the signs and symptoms of CLN3 disease.

CLN3 disease is characterized by the accumulation of proteins and other substances in lysosomes. These accumulations occur in cells throughout the body; however, nerve cells seem to be particularly vulnerable to their effects. The accumulations can cause cell damage leading to cell death. The progressive death of nerve cells in the brain and other tissues leads to the neurological signs and symptoms of CLN3 disease. However, it is unclear how mutations in the CLN3 gene are involved in the buildup of substances in lysosomes.

2.2. Other Disorders

Mutations in the CLN3 gene can cause vision impairment without the other signs and symptoms of CLN3 disease (described above), which is known as CLN3-associated isolated retinal degeneration. In affected individuals, vision impairment is caused by a breakdown of the light-sensitive tissue at the back of the eye (retinal degeneration). People with CLN3-associated isolated retinal degeneration typically have decreased sharpness of vision (visual acuity) and increased sensitivity to light (photophobia). There are two types of this condition, which are distinguished by the age at which vision problems begin. The early-onset form begins in late childhood or adolescence, and the late-onset form begins in early to mid-adulthood.

Research suggests that the CLN3 gene mutations that cause CLN3-associated isolated retinal degeneration are less severe than those that cause CLN3 disease. As a result, a partially functional CLN3 protein is produced, which leads to the development of visual problems in affected individuals without the neurological features characteristic of CLN3 disease.

3. Other Names for This Gene

  • BATTENIN
  • BTN1
  • BTS
  • ceroid-lipofuscinosis, neuronal 3
  • CLN3_HUMAN
  • JNCL
  • MGC102840

This entry is adapted from https://medlineplus.gov/genetics/gene/cln3

References

  1. Cotman SL, Staropoli JF. The juvenile Batten disease protein, CLN3, and itsrole in regulating anterograde and retrograde post-Golgi trafficking. ClinLipidol. 2012 Feb;7(1):79-91.
  2. Cárcel-Trullols J, Kovács AD, Pearce DA. Cell biology of the NCL proteins:What they do and don't do. Biochim Biophys Acta. 2015 Oct;1852(10 Pt B):2242-55. doi: 10.1016/j.bbadis.2015.04.027.
  3. Kitzmüller C, Haines RL, Codlin S, Cutler DF, Mole SE. A function retained by the common mutant CLN3 protein is responsible for the late onset of juvenileneuronal ceroid lipofuscinosis. Hum Mol Genet. 2008 Jan 15;17(2):303-12.
  4. Ku CA, Hull S, Arno G, Vincent A, Carss K, Kayton R, Weeks D, Anderson GW,Geraets R, Parker C, Pearce DA, Michaelides M, MacLaren RE, Robson AG, Holder GE,Heon E, Raymond FL, Moore AT, Webster AR, Pennesi ME. Detailed Clinical Phenotypeand Molecular Genetic Findings in CLN3-Associated Isolated Retinal Degeneration. JAMA Ophthalmol. 2017 Jul 1;135(7):749-760. doi:10.1001/jamaophthalmol.2017.1401.
  5. Mirza M, Vainshtein A, DiRonza A, Chandrachud U, Haslett LJ, Palmieri M,Storch S, Groh J, Dobzinski N, Napolitano G, Schmidtke C, Kerkovich DM. The CLN3 gene and protein: What we know. Mol Genet Genomic Med. 2019 Dec;7(12):e859. doi: 10.1002/mgg3.859.
  6. Oetjen S, Kuhl D, Hermey G. Revisiting the neuronal localization andtrafficking of CLN3 in juvenile neuronal ceroid lipofuscinosis. J Neurochem. 2016Nov;139(3):456-470. doi: 10.1111/jnc.13744.
  7. Phillips SN, Benedict JW, Weimer JM, Pearce DA. CLN3, the protein associatedwith batten disease: structure, function and localization. J Neurosci Res. 2005Mar 1;79(5):573-83. Review.
  8. Rakheja D, Narayan SB, Bennett MJ. The function of CLN3P, the Batten diseaseprotein. Mol Genet Metab. 2008 Mar;93(3):269-74. Review. Erratum in: Mol GenetMetab. 2008 Jun;94(2):270.
  9. Uusi-Rauva K, Kyttälä A, van der Kant R, Vesa J, Tanhuanpää K, Neefjes J,Olkkonen VM, Jalanko A. Neuronal ceroid lipofuscinosis protein CLN3 interactswith motor proteins and modifies location of late endosomal compartments. CellMol Life Sci. 2012 Jun;69(12):2075-89. doi: 10.1007/s00018-011-0913-1.
More
Information
Contributor:
View Times: 37
Entry Collection: MedlinePlus
Revision: 1 times (View History)
Update Time: 24 Dec 2020
Table of Contents

    Confirm

    Are you sure to Delete?

    Video Upload Options

    Do you have a full video?
    Cite
    If you have any further questions, please contact Encyclopedia Editorial Office.
    Zhou, V. CLN3 Gene. Encyclopedia. Available online: https://encyclopedia.pub/entry/5151 (accessed on 22 May 2022).
    Zhou V. CLN3 Gene. Encyclopedia. Available at: https://encyclopedia.pub/entry/5151. Accessed May 22, 2022.
    Zhou, Vicky. "CLN3 Gene," Encyclopedia, https://encyclopedia.pub/entry/5151 (accessed May 22, 2022).
    Zhou, V. (2020, December 24). CLN3 Gene. In Encyclopedia. https://encyclopedia.pub/entry/5151
    Zhou, Vicky. ''CLN3 Gene.'' Encyclopedia. Web. 24 December, 2020.
    Share
    Download
    Cite
    Top