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Germline mutations directions are different between introns of the same gene: case study of the gene coding for amyloid-beta precursor proteinстатья
Дата последнего поиска статьи во внешних источниках: 1 мая 2024 г.
- Авторы: Khrustalev Vladislav Victorovich, Khrustaleva Tatyana Aleksandrovna, Popinako Anna Vladimirovna
- Журнал: Genetica
- Том: 151
- Номер: 1
- Год издания: 2022
- Издательство: Springer Nature
- Местоположение издательства: Switzerland
- Первая страница: 61
- Последняя страница: 73
- DOI: 10.1007/s10709-022-00166-6
- Аннотация: Amyloid-beta precursor protein (APP) is highly conserved in mammals. This feature allowed us to compare nucleotide usage biases in fourfold degenerated sites along the length of its coding region for 146 species of mammals and birds in search of fragments with significant deviations. Even though cytosine usage has the highest value in fourfold degenerated sites in APP coding region from all tested placental mammals, in contrast to marsupial mammals with the bias toward thymine usage, the most frequent germline and somatic mutations in human APP coding region are C to T and G to A transitions. The same mutational AT-pressure is characteristic for germline mutations in introns of human APP gene. However, surprisingly, there are several exceptional introns with deviations in germline mutations rates. The most of those introns surround exons with exceptional biases in nucleotide usage in fourfold degenerated sites. Existence of such fragments in exons 4 and 5, as well as in exon 14, can be connected with the presence of lncRNA genes in complementary strand of DNA. Exceptional nucleotide usage bias in exons 16 and 17 that contain a sequence encoding amyloid-beta peptides can be explained either by the presence of yet unmapped lncRNA(s), or by the autonomous expression of a short mRNA that encodes just C-terminal part of the APP providing an alternative source of amyloid-beta peptides. This hypothesis is supported by the increased rate of T to C transitions in introns 16-17 and 17-18 of Human APP gene relatively to other introns.Keywords: Amyloid-beta precursor protein; Autonomous transcription; Beta-amyloid peptides; Germline mutations; Mutational pressure.
- Добавил в систему: Попинако Анна Владимировна