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Article

Alpha-Thalassemia in Southern Italy: Characterization of Five New Deletions Removing the Alpha-Globin Gene Cluster

1
Institute of Genetics and Biophysics “Adriano Buzzati Traverso” (IGB-ABT, CNR), National Research Council, 80131 Napoli, Italy
2
Department of Precision Medicine, University of Campania L. Vanvitelli, 80138 Napoli, Italy
3
Telethon Institute of Genetics and Medicine (TIGEM), 80078 Pozzuoli, Italy
*
Author to whom correspondence should be addressed.
Int. J. Mol. Sci. 2023, 24(3), 2577; https://doi.org/10.3390/ijms24032577
Submission received: 24 December 2022 / Revised: 25 January 2023 / Accepted: 26 January 2023 / Published: 30 January 2023
(This article belongs to the Collection Feature Papers in Molecular Genetics and Genomics)

Abstract

α-thalassemia is characterized in about 80% of cases by deletions generated by the presence of duplications and interspersed repeated sequences in the α-globin gene cluster. In a project on the molecular basis of α-thalassemia in Southern Italy, we identified six families, showing an absence of the most common deletions, and normal α-globin gene sequences. Multiplex Ligation-dependent Probe Amplification (MLPA), qRT-PCR, and the sequencing of long-range PCR amplicon have been used for the identification and characterization of new deletions. MLPA analysis for the identification of α- and β-globin rearrangement revealed the presence of five new α-thalassemia deletions. The set-up of qRT-PCR allowed us to delimit the extent of the deletions ranging from about 10 kb to more than 250 kb, two of them being of the telomeric type. The long-range PCR generated a specific anomalous fragment in three deletions, and only several unspecific bands in the other two deletions. The sequencing of the anomalous amplicons revealed the breakpoints of two deletions: the --PA, 34 kb long, identified in two families, and the telomeric --AG, 274 kb long. The anomalous fragment containing the breakpoint of the deletion --FG was partially sequenced, and it was not possible to identify the breakpoints due to the presence of several repetitive Alu sequences. The analysis of the breakpoint regions of the --Sciacca and --Puglia, respectively, are about 10 and 165 kb long, and revealed the presence of repeats that most likely impaired the amplification of a specific fragment for the identification of the breakpoint. MLPA, in association with qRT-PCR and long-range PCR, is a good approach for the identification and molecular characterization of rare or new deletions. Breakpoint analysis confirms that Alu sequences play an important role in favoring unequal crossing-over. Southern Italy shows considerable genetic heterogeneity, as expected with its central position in the Mediterranean basin, favoring migratory flows.
Keywords: alpha-thalassemia; MLPA; qRT-PCR; deletion breakpoint characterization; --Sciacca; --FG; --PA; --Puglia; --AG alpha-thalassemia; MLPA; qRT-PCR; deletion breakpoint characterization; --Sciacca; --FG; --PA; --Puglia; --AG

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MDPI and ACS Style

Cardiero, G.; Musollino, G.; Prezioso, R.; Nigro, V.; Lacerra, G. Alpha-Thalassemia in Southern Italy: Characterization of Five New Deletions Removing the Alpha-Globin Gene Cluster. Int. J. Mol. Sci. 2023, 24, 2577. https://doi.org/10.3390/ijms24032577

AMA Style

Cardiero G, Musollino G, Prezioso R, Nigro V, Lacerra G. Alpha-Thalassemia in Southern Italy: Characterization of Five New Deletions Removing the Alpha-Globin Gene Cluster. International Journal of Molecular Sciences. 2023; 24(3):2577. https://doi.org/10.3390/ijms24032577

Chicago/Turabian Style

Cardiero, Giovanna, Gennaro Musollino, Romeo Prezioso, Vincenzo Nigro, and Giuseppina Lacerra. 2023. "Alpha-Thalassemia in Southern Italy: Characterization of Five New Deletions Removing the Alpha-Globin Gene Cluster" International Journal of Molecular Sciences 24, no. 3: 2577. https://doi.org/10.3390/ijms24032577

APA Style

Cardiero, G., Musollino, G., Prezioso, R., Nigro, V., & Lacerra, G. (2023). Alpha-Thalassemia in Southern Italy: Characterization of Five New Deletions Removing the Alpha-Globin Gene Cluster. International Journal of Molecular Sciences, 24(3), 2577. https://doi.org/10.3390/ijms24032577

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