| Title: |
The role of ClpX in erythropoietic protoporphyria |
| Authors: |
Whitman, Jared C., Paw, Barry H., Chung, Jacky |
| Source: |
Hematology, Transfusion and Cell Therapy. June 2018 40(2) |
| Publisher Information: |
Associação Brasileira de Hematologia, Hemoterapia e Terapia Celular (ABHH), 2018. |
| Publication Year: |
2018 |
| Subject Terms: |
Heme biosynthesis enzymes, Porphyria, Erythropoietic protoporphyria, ClpXP, ALAS gene |
| More Details: |
Hemoglobin is an essential biological component of human physiology and its production in red blood cells relies upon proper biosynthesis of heme and globin protein. Disruption in the synthesis of these precursors accounts for a number of human blood disorders found in patients. Mutations in genes encoding heme biosynthesis enzymes are associated with a broad class of metabolic disorders called porphyrias. In particular, one subtype – erythropoietic protoporphyria – is caused by the accumulation of protoporphyrin IX. Erythropoietic protoporphyria patients suffer from photosensitivity and a higher risk of liver failure, which is the principle cause of morbidity and mortality. Approximately 90% of these patients carry loss-of-function mutations in the enzyme ferrochelatase (FECH), while 5% of cases are associated with activating mutations in the C-terminus of ALAS2. Recent work has begun to uncover novel mechanisms of heme regulation that may account for the remaining 5% of cases with previously unknown genetic basis. One erythropoietic protoporphyria family has been identified with inherited mutations in the AAA+ protease ClpXP that regulates ALAS activity. In this review article, recent findings on the role of ClpXP as both an activating unfoldase and degrading protease and its impact on heme synthesis will be discussed. This review will also highlight the role of ClpX dysfunction in erythropoietic protoporphyria. |
| Document Type: |
article |
| File Description: |
text/html |
| Language: |
English |
| ISSN: |
2531-1379 |
| DOI: |
10.1016/j.htct.2018.03.001 |
| Access URL: |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S2531-13792018000200182 |
| Rights: |
info:eu-repo/semantics/openAccess |
| Accession Number: |
edssci.S2531.13792018000200182 |
| Database: |
SciELO |
