» Articles » PMID: 3486422

Complete Nucleotide Sequence of Two Steroid 21-hydroxylase Genes Tandemly Arranged in Human Chromosome: a Pseudogene and a Genuine Gene

Overview
Specialty Science
Date 1986 May 1
PMID 3486422
Citations 126
Authors
Affiliations
Soon will be listed here.
Abstract

Two 21-hydroxylase [P-450(C21)] genes have been isolated from a human genomic library using a bovine P-450(C21) cDNA. The insert DNAs containing the P-450(C21) genes were also hybridized with the sequences of the 5' or 3' end regions of human C4 cDNA, indicating a close linkage of the P-450(C21) gene to the C4 gene. Sequence analysis has revealed that the two P-450(C21) genes are both approximately equal to 3.4 kilobases long and split into 10 exons. Comparing the two sequences, we found that the two genes are highly homologous including their introns and flanking sequences, but that three mutations render one of the two P-450(C21) genes nonfunctional--1 base insertion, an 8-base deletion, and a transition mutation--all of which may cause premature termination of the translation. Tandem arrangement of the highly homologous pseudo- and genuine genes in close proximity could account for the high incidence of P-450(C21) gene deficiency by homologous gene recombination.

Citing Articles

Genetics in Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency and Clinical Implications.

Concolino P, Falhammar H J Endocr Soc. 2025; 9(3):bvaf018.

PMID: 39911519 PMC: 11795198. DOI: 10.1210/jendso/bvaf018.


Clinical Manifestations and Treatment Challenges in Infants and Children With Classic Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency.

Nokoff N, Buchanan C, Barker J J Clin Endocrinol Metab. 2025; 110(Supplement_1):S13-S24.

PMID: 39836622 PMC: 11749889. DOI: 10.1210/clinem/dgae563.


Genetics and Pathophysiology of Classic Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency.

Yang M, White P J Clin Endocrinol Metab. 2025; 110(Supplement_1):S1-S12.

PMID: 39836621 PMC: 11749890. DOI: 10.1210/clinem/dgae535.


High clinical utility of long-read sequencing for precise diagnosis of congenital adrenal hyperplasia in 322 probands.

Wang Y, Zhu G, Li D, Pan Y, Li R, Zhou T Hum Genomics. 2025; 19(1):3.

PMID: 39810276 PMC: 11731552. DOI: 10.1186/s40246-024-00696-4.


Long-Read Sequencing Identifying the Genetic Complexity of Congenital Adrenal Hyperplasia in the Pedigree.

Chen X, Zhao J, Li D, Xi N, Yi D, Yan M Mol Genet Genomic Med. 2024; 12(11):e70029.

PMID: 39575462 PMC: 11582476. DOI: 10.1002/mgg3.70029.


References
1.
Southern E . Detection of specific sequences among DNA fragments separated by gel electrophoresis. J Mol Biol. 1975; 98(3):503-17. DOI: 10.1016/s0022-2836(75)80083-0. View

2.
Hood L, Steinmetz M, Malissen B . Genes of the major histocompatibility complex of the mouse. Annu Rev Immunol. 1983; 1:529-68. DOI: 10.1146/annurev.iy.01.040183.002525. View

3.
Lawn R, Fritsch E, Parker R, Blake G, Maniatis T . The isolation and characterization of linked delta- and beta-globin genes from a cloned library of human DNA. Cell. 1978; 15(4):1157-74. DOI: 10.1016/0092-8674(78)90043-0. View

4.
Slightom J, Blechl A, SMITHIES O . Human fetal G gamma- and A gamma-globin genes: complete nucleotide sequences suggest that DNA can be exchanged between these duplicated genes. Cell. 1980; 21(3):627-38. DOI: 10.1016/0092-8674(80)90426-2. View

5.
Kioussis D, Eiferman F, van de Rijn P, Gorin M, Ingram R, Tilghman S . The evolution of alpha-fetoprotein and albumin. II. The structures of the alpha-fetoprotein and albumin genes in the mouse. J Biol Chem. 1981; 256(4):1960-7. View