scholarly journals Human angiotensin I-converting enzyme gene and endurance performance

1999 ◽  
Vol 87 (4) ◽  
pp. 1313-1316 ◽  
Author(s):  
Saul Myerson ◽  
Harry Hemingway ◽  
Richard Budget ◽  
John Martin ◽  
Steve Humphries ◽  
...  

Human physical performance is strongly influenced by genetic factors. A variation in the structure of the human angiotensin I-converting enzyme (ACE) gene has been reported in which the insertion (I) variant is associated with lower ACE levels than the deletion (D) gene. We have previously reported that the I variant was associated with improved endurance performance in high-altitude mountaineers and British Army recruits. We now examine this genotype distribution in 91 British Olympic-standard runners (79 Caucasians). DNA was extracted from the buccal cells contained in 10 ml of saline mouthwash donated by the subjects, and the I and D variants of the ACE gene were identified by PCR amplification of the polymorphic region. There was an increasing frequency of the I allele with distance run [0.35, 0.53, and 0.62 for ≤200 m ( n = 20), 400–3,000 m ( n = 37), and ≥5,000 m ( n = 34), respectively; P = 0.009 for linear trend]. Among 404 Olympic-standard athletes from 19 other mixed sporting disciplines (in which endurance performance was not necessarily a key factor), the I allele did not differ significantly from that found in control subjects: 0.50 vs. 0.49 ( P = 0.526). These results support a positive association of the I allele with elite endurance performance.

2008 ◽  
Vol 397 (1-2) ◽  
pp. 65-67 ◽  
Author(s):  
Marco Antonio Martínez-Ríos ◽  
Marco Antonio Peña-Duque ◽  
José Manuel Fragoso ◽  
Hilda Delgadillo-Rodríguez ◽  
Nonanzit Pérez-Hernández ◽  
...  

1996 ◽  
Vol 17 (1) ◽  
pp. 27-30 ◽  
Author(s):  
S Ueda ◽  
R P Heeley ◽  
K. R Lees ◽  
H L Elliott ◽  
J M C Connell

ABSTRACT A polymorphism of the gene encoding the human angiotensin I-converting enzyme (ACE), which is defined by an insertion/deletion polymorphism in intron 16, has been identified as a candidate genetic locus in the development of cardiovascular and renal disease. We have demonstrated that the accuracy of ACE genotyping is critically dependent on the strategy of the PCR used in typing. Of 1238 individuals genotyped by a standard method, 335 were typed as DD, 645 as DI and 258 as II. However, when DD individuals were retyped using modified methods (including either 5% dimethyl sulphoxide, or a 'hot start') 35 of the original 335 samples (10·5%) were retyped as DI. In approximately half of these mistyped samples, PCR amplification was assessed as inefficient by the absence of a third faint heteroduplex band in a control ID sample: when the assay was repeated without any modifications, the mistyped samples were correctly genotyped. In the remainder, mistyping persisted. In these cases, the use of a third 'nested' PCR primer specific for the I allele was required for successful genotyping, providing a more reliable strategy without the need for further modification to the PCR technique. Our results suggest that the triple primer approach is the method of choice for accurate ACE genotyping.


2003 ◽  
Vol 35 (Supplement 1) ◽  
pp. S184
Author(s):  
T Tobina ◽  
R Michishita ◽  
N Matsuhira ◽  
B Zhang ◽  
K Saku ◽  
...  

Thorax ◽  
1996 ◽  
Vol 51 (8) ◽  
pp. 777-780 ◽  
Author(s):  
K. Furuya ◽  
E. Yamaguchi ◽  
A. Itoh ◽  
N. Hizawa ◽  
N. Ohnuma ◽  
...  

1993 ◽  
Vol 290 (1) ◽  
pp. 33-40 ◽  
Author(s):  
O Costerousse ◽  
J Allegrini ◽  
M Lopez ◽  
F Alhenc-Gelas

The expression of angiotensin-I converting enzyme (ACE; EC 3.4.15.1) in human circulating mononuclear cells was studied. T-lymphocytes contained the highest level of enzyme, approx. 28 times more per cell than monocytes. No activity was detected in B-lymphocytes. ACE was present mainly in the microsomal fraction, where it was found to be the major membrane-bound bradykinin-inactivating enzyme. An mRNA for ACE was detected and characterized after reverse transcription and amplification by PCR in T-lymphocytes and several T-cell leukaemia cell lines. We have previously observed that the interindividual variability in the levels of ACE in plasma is, in part, genetically determined and influenced by an insertion/deletion polymorphism of the ACE gene. To investigate the mechanisms involved in the regulation of ACE biosynthesis, the ACE levels of T-lymphocytes from 35 healthy subjects having different ACE genotypes were studied. These levels varied widely between individuals but were highly reproducible and influenced by the polymorphism of the ACE gene. T-lymphocyte levels of ACE were significantly higher in subjects who were homozygote for the deletion than in the other subjects. These results show that ACE is expressed in T-lymphocytes and indicate that the level of ACE expression in cells synthesizing the enzyme is genetically determined.


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