The SUCLG1 gene encodes the alpha-subunit of the GDP-forming succinate-CoA
ligase (alternative name: succinyl-CoA synthetase (SCS)). SCS is a mitochondrial
matrix enzyme catalyzing the reversible synthesis of succinyl-CoA and either
ADP or GDP to succinate and either ATP of GTP, depending on which beta-subunit
is present, in the Krab cycle. This dimeric enzyme consists of one alpha subunit
and one of two beta units encoded either by SUCLA2 (test code 3375) (ATP/ADP
specific) or SUCLG2 (GTP/GDP specific). Thus, the beta subunit determines substrate
specificity for either the GTP-dependent or ATP-dependent reactions. One mutation
of 2-bp homozygous deletion in SUCLG1 has been identified in a consanguineous
Pakistani family with fatal infantile lactic acidosis and mitochondrial DNA
depletion. The clinical symptoms of SUCLG1 mutation are similar to those of
SUCLA2 mutations. Elevated levels of lactate, pyruvate, methylmalonate and
methylcitrate in urine suggest a deficiency of SCS. The human SUCLG1 gene is
located at 2p11.2 and contains 9 coding exons encoding 333 amino acids.
-
Confirmation of a clinical diagnosis
- Carrier testing
- Prenatal diagnosis for known familial mutations
The exons and flanking intronic regions of the SUCLG1 gene
are PCR amplified and sequenced in both the forward and reverse directions.
Blood: EDTA (purple-top)
tubes: Adult: 14
cc; Child: 6 cc; Infant: 2-3 cc
Requisition form must accompany the specimen. To receive forms,
additional information or specimen collection kits, please contact the
laboratory. Please call laboratory for specific requirements for
prenatal testing.
Index: 4 weeks
Known Familial Mutation: 2 weeks
Index: 83891, 83904x18, 83898x9, 83912, 83894x2
Known Familial Mutation: 83904x4, 83898x2,
83912, 83891, 83894x2
>> Gene
Sequencing
Requisition
>> Prenatal
Requisition
2. Ostergaard
E, Christensen
E, Kristensen
E, Mogensen
B, Duno
M, Shoubridge
EA, Wibrand
F. Deficiency of the alpha subunit of succinate-coenzyme A ligase
causes fatal infantile lactic acidosis with mitochondrial DNA depletion.
Am J Hum Genet. 81(2):383-7, 2007
Last Modified: 5-28-08
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