Flexing DNA: HMG-box proteins and their partners

Article Abstract:

High-mobility group (HMG)-box proteins and partners are discussed from the perspective of the realization of recent years that DNA and transcription factors form a tight-knit 3-D arrangement with bends, twists and many internal protein contacts so that transcription factors are in touch, perhaps several of them. SRY, the best known of DNA-flexing proteins, is very likely to have a partner and likely interacts with it in its HMG box, and is considered with HMG1 and relatives and the building up of targeting specificity.

author: Bianchi, Marco E., Beltrame, Monica
Analysis, Physiological aspects, DNA, Proteins, Genetic regulation, Genetic transcription, Transcription (Genetics), RNA polymerases, Homeobox genes, Cell nuclei, Cell nucleus, Protein structure, Sex determination, Genetic, Sex determination (Genetics)

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Genotype-phenotype relationships in ataxia-telangiectasia and variants

Article Abstract:

Ataxia-telangiectasia (A-T) has ATM as the underlying gene. It encodes a large protein kinase with a phosphatidylinositol 3-kinase-like domain. ATM protein levels have been measured in six A-T variants and the ATM genes searched for mutations. Findings show there is a larger range of phenotypes associated with ATM mutations than had been known and show that some A-T variant phenotypes come from ATM mutations. Some of those are without telangiectasia. A-T is a complex multisystem autosomal recessive disorder.

author: Gatti, Richard A., Shiloh, Yosef, Russell, Pamela, Khosravi, Rami, Chessa, Luciana, Gilad, Shlomit, Galanty, Yaron, Piane, Maria, Jorgensen, Timothy J., Bar-Shira, Anat
Israel, Cellular signal transduction

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Ataxia-telangiectasia: identification and detection of founder-effect mutations in the ATM gene in ethnic populations

Article Abstract:

Ten ethnic populations have been studied to determine common mutations in the ATM gene associated with ataxia-telangiectasia (A-T). Ninety-two truncating mutations were found by screening 140 mutant alleles. Founder-effect mutations were found in Costa Rican, Norwegian, Polish, Italian and Amish/Mennonite populations. Genomic mutations and effects on cDNA were examined to enable assessment of ATM heterozygotes in relation to susceptibility to other diseases.

author: Gatti, Richard A., Castellvi-Bel, Sergi, Concannon, Patrick, Telatar, Milhan, Teraoka, Sharon, Wang, Zhijun, Chun, Helen H., Liang, Teresa, Udar, Nitin, Borressen-Dale, Anne-Lise, Chessa, Luciana, Bernatowska-Matuszkiewicz, Eva, Porras, Oscar, Watanabe, Mitsunori, Junker, Anne
Human population genetics

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subjects list: Research, Italy, United States, Usage, Genetic aspects, Chromosome mapping, Genetic disorders, Ataxia telangiectasia
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