• HOME
  • NEWS
  • EXPLORE
    • CAREER
      • Companies
      • Jobs
    • EVENTS
    • iGEM
      • News
      • Team
    • PHOTOS
    • VIDEO
    • WIKI
  • BLOG
  • COMMUNITY
    • FACEBOOK
    • INSTAGRAM
    • TWITTER
Saturday, October 4, 2025
BIOENGINEER.ORG
No Result
View All Result
  • Login
  • HOME
  • NEWS
  • EXPLORE
    • CAREER
      • Companies
      • Jobs
        • Lecturer
        • PhD Studentship
        • Postdoc
        • Research Assistant
    • EVENTS
    • iGEM
      • News
      • Team
    • PHOTOS
    • VIDEO
    • WIKI
  • BLOG
  • COMMUNITY
    • FACEBOOK
    • INSTAGRAM
    • TWITTER
  • HOME
  • NEWS
  • EXPLORE
    • CAREER
      • Companies
      • Jobs
        • Lecturer
        • PhD Studentship
        • Postdoc
        • Research Assistant
    • EVENTS
    • iGEM
      • News
      • Team
    • PHOTOS
    • VIDEO
    • WIKI
  • BLOG
  • COMMUNITY
    • FACEBOOK
    • INSTAGRAM
    • TWITTER
No Result
View All Result
Bioengineer.org
No Result
View All Result
Home NEWS Science News Biology

Retinitis pigmentosa research probes role of the enzyme DHDDS in this genetic disease

Bioengineer by Bioengineer
June 11, 2020
in Biology
Reading Time: 4 mins read
0
IMAGE
Share on FacebookShare on TwitterShare on LinkedinShare on RedditShare on Telegram

Results show that retinitis pigmentosa 59 may not be a congenital disorder of glycosylation, as was long assumed

IMAGE

Credit: UAB

BIRMINGHAM, Ala. – Researchers who made a knock-in mouse-model of the genetic disorder retinitis pigmentosa 59, or RP59, expected to see retinal degeneration and retinal thinning. As reported in the journal Cells, they surprisingly found none, calling into question the commonly accepted — though never proved — mechanism for RP59.

“Our findings bring into question the current concept that RP59 is a member of a large and diverse class of diseases known as ‘congenital disorders of glycosylation,'” said Steven Pittler, Ph.D., professor and director of the University of Alabama at Birmingham School of Optometry and Vision Science Vision Science Research Center. “While in principle it would be reasonable to consider RP59 as a congenital disorder of glycosylation, due to the associated mutation in DHDDS, an enzyme required for glycosylation, there is no direct evidence to demonstrate a glycosylation defect in the human retinal disease or in any animal model of RP59 generated to date.”

This means the mechanism of DHDDS-dependent retinal degeneration in human RP59 patients remains unknown, and appears to be more complex than just a DHDDS loss of function.

Retinitis pigmentosa is a group of rare genetic disorders affecting the light-sensitive retinal tissue at the back of the eye. Patients first notice night blindness and loss of peripheral vision, and the disease can progress to vision loss and legal blindness. RP59 has changes in the gene for DHDDS, one of the 50 genes that can lead to RP. RP59 is found in one in 100 Ashkenazi Jewish people and one in 2,009 people worldwide.

In RP59, the lysine that is the 42nd amino acid of the DHDDS enzyme is changed to a glutamic acid, a change known as a K42E point mutation. So Pittler and colleagues at UAB and the State University of New York at Buffalo, or SUNY-Buffalo, examined the retinas of mice that were made homozygous for a DHDDS K42E mutation.

Using spectral domain-optical coherence tomography, they found no evidence of retinal degeneration, even up to one year of age. Also, there was no evidence of compromised protein N-glycosylation, meaning there was no significant DHDDS loss of function in the K42E mice. Opsin, a protein in photoreceptor cells involved in vision, is often mislocalized when photoreceptor cells degenerate; however, the K42E mice showed no change in opsin localization.

What the researchers did find was extensive gliosis in the retinas of the mutant mice, which was spread in a radial pattern throughout the inner retinal layers to the outer plexiform layer of the retina. There was also intense gliosis at the vitreoretinal interface. Gliosis is a change in glial cells of the central nervous system, often in response to injury. In the retina, it affects glial M?ller cells, and that reactive gliosis can have harmful effects on vision.

“These results indicate massive gliotic activation,” Pittler said, “which is remarkable considering the lack of overt retinal degeneration or loss of retinal neurons.”

###

The study, “Lack of overt retinal degeneration in a K42E Dhdds knock-in mouse model of RP59,” is published in Cells. Co-authors with Pittler are Sriganesh Ramachandra Rao and Steven J. Fliesler, SUNY-Buffalo; and Pravallika Kotla and Mai N. Nguyen, UAB Department of Optometry and Vision Science.

Support came from National Institutes of Health grants EY029341 and P30 003039; a Fight for Sight Summer Student Fellowship, a Career-Starter Research Grant from the Knights Templar Eye Foundation, the UAB Vision Science Research Center and the Veterans Affairs Western New York Healthcare System.

Pittler and colleagues have also published two companion papers that further probe the role of DHDDS in RP.

The first study, “Selective ablation of dehydrodolichol diphosphate synthase in murine retinal pigment epithelium causes RPE atrophy and retinal degeneration,” is published in Cells. It showed that retinal pigment epithelium-specific deletion of the gene for DHDDS in mice induced structural and functional deficits in the retinal pigment epithelium and the photoreceptors. This suggests that retinal pigment epithelium pathology may be a significant contributor to the retinal degeneration observed in humans with RP59 mutations.

Researchers at UAB and SUNY-Buffalo did the study.

The second study, “Retinal degeneration caused by rod-specific Dhdds ablation occurs without concomitant inhibition of protein N-glycosylation,” is published in IScience. It examined the rod photoreceptor-specific ablation of the gene for DHDDS. The researchers found that mouse retinas had mild retinal dysfunction at four weeks after birth, followed by rapid photoreceptor degeneration and almost complete loss of rods and cones by six weeks after birth. Rods and cones are the photoreceptors of the retina. Retinal proteins, including opsin, still showed N-glycosylation, which again challenges the conventional mechanistic view of RP59 as a congenital disorder of glycosylation.

Researchers at UAB, SUNY-Buffalo and the Polish Academy of Sciences did the study.

Media Contact
Jeff Hansen
[email protected]

Original Source

https://www.uab.edu/news/research/item/11364-retinitis-pigmentosa-research-probes-role-of-the-enzyme-dhdds-in-this-genetic-disease

Related Journal Article

http://dx.doi.org/10.3390/cells9040896

Tags: Cell BiologyMedicine/HealthneurobiologyOphthalmologyPhysiology
Share13Tweet8Share2ShareShareShare2

Related Posts

blank

Revolutionary Graph Network Enhances Protein Interaction Prediction

October 4, 2025
DOG Gene Family in Wheat Drives Seed Dormancy

DOG Gene Family in Wheat Drives Seed Dormancy

October 4, 2025

Discovery of MrSTP20: Sugar Transporter in Salt Stress

October 4, 2025

SNARE Neofunctionalization Driven by Vacuole Retrieval

October 4, 2025
Please login to join discussion

POPULAR NEWS

  • New Study Reveals the Science Behind Exercise and Weight Loss

    New Study Reveals the Science Behind Exercise and Weight Loss

    93 shares
    Share 37 Tweet 23
  • New Study Indicates Children’s Risk of Long COVID Could Double Following a Second Infection – The Lancet Infectious Diseases

    90 shares
    Share 36 Tweet 23
  • Physicists Develop Visible Time Crystal for the First Time

    75 shares
    Share 30 Tweet 19
  • New Insights Suggest ALS May Be an Autoimmune Disease

    69 shares
    Share 28 Tweet 17

About

We bring you the latest biotechnology news from best research centers and universities around the world. Check our website.

Follow us

Recent News

Gut Microbiome and Hormones in Postmenopausal Breast Cancer

Herbal Remedies for Hypertension: Insights from Trinidad

Revolutionary Graph Network Enhances Protein Interaction Prediction

Subscribe to Blog via Email

Success! An email was just sent to confirm your subscription. Please find the email now and click 'Confirm' to start subscribing.

Join 62 other subscribers
  • Contact Us

Bioengineer.org © Copyright 2023 All Rights Reserved.

Welcome Back!

Login to your account below

Forgotten Password?

Retrieve your password

Please enter your username or email address to reset your password.

Log In
No Result
View All Result
  • Homepages
    • Home Page 1
    • Home Page 2
  • News
  • National
  • Business
  • Health
  • Lifestyle
  • Science

Bioengineer.org © Copyright 2023 All Rights Reserved.