Evidence map›Paper›PMID 36768900›Full record

ArticleInternational journal of molecular sciences2023

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

Giovanna Cardiero, Gennaro Musollino, Romeo Prezioso, Vincenzo Nigro, Giuseppina Lacerra

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Article in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

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3citing papers in PubMed
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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Giovanna CardieroInstitute of Genetics and Biophysics "Adriano Buzzati Traverso" (IGB-ABT, CNR), National Research Council, 80131 Napoli, Italy.
Gennaro MusollinoInstitute of Genetics and Biophysics "Adriano Buzzati Traverso" (IGB-ABT, CNR), National Research Council, 80131 Napoli, Italy.
Romeo PreziosoInstitute of Genetics and Biophysics "Adriano Buzzati Traverso" (IGB-ABT, CNR), National Research Council, 80131 Napoli, Italy.
Vincenzo NigroDepartment of Precision Medicine, University of Campania L. Vanvitelli, 80138 Napoli, Italy.
Giuseppina LacerraInstitute of Genetics and Biophysics "Adriano Buzzati Traverso" (IGB-ABT, CNR), National Research Council, 80131 Napoli, Italy.ORCID 0000-0003-1038-8363

Funding

Ministry of Education, Universities and Research Legge 488/92 (Cluster C02, Project 2)
6 · The paper itself

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.

Indexed as

alpha-Thalassemiaalpha-GlobinsHumansItalyMultigene FamilyMultiplex Polymerase Chain Reactionalpha-Globins--AGalpha-thalassemiadeletion breakpoint characterization--FGMLPA--PA--PugliaqRT-PCR--Sciacca

Identifiers

PMID36768900
PMCPMC9916800

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