Literature DB >> 8707297

A LINE element is present at the site of a 300-kb deletion starting in intron 10 of the PAX6 gene in a case of familial aniridia.

M Drechsler1, B Royer-Pokora.   

Abstract

We have identified a 300-kb germline deletion in 11p13 in a family with aniridia but no Wilms' tumor. Cloning and sequencing of the breakpoint revealed that the deletion starts in intron 10 of the PAX6 gene and removes the C-terminal part of the proline-serine-threonine rich domain, leaving both DNA-binding domains intact. The PAX6 gene is joined head-to-head to a LINE-1 (L1) element. The L1 is truncated at the 3' end, removing part of ORF2. Sequencing of the L1 element shows that it does not encode a functional transposase and is therefore probably not an active element. These data suggest that the L1 element is normally present at the site of the distal deletion endpoint in 11p13. No extensive sequence homologies are detected at the deletion junction points; however, the PAX6 gene as well as the L1 element have runs of T nucleotides at this position, indicating that the deletion occurred by nonhomologous recombination. Several consensus recognition sequences for topoisomerase I flank the deletion site in both sequences, suggesting an involvement of this enzyme during the deletion-recombination process.

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Year:  1996        PMID: 8707297     DOI: 10.1007/s004390050210

Source DB:  PubMed          Journal:  Hum Genet        ISSN: 0340-6717            Impact factor:   4.132


  10 in total

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2.  Novel endogenous type D retroviral particles expressed at high levels in a SCID mouse thymic lymphoma.

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3.  Sequence of the FRA3B common fragile region: implications for the mechanism of FHIT deletion.

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4.  Two novel mutations of the PAX6 gene causing different phenotype in a cohort of Chinese patients.

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5.  A 117-kb microdeletion removing HOXD9-HOXD13 and EVX2 causes synpolydactyly.

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6.  Large novel deletions detected in Chinese families with aniridia: correlation between genotype and phenotype.

Authors:  Xiaohui Zhang; Qingsheng Zhang; Yi Tong; Hanjun Dai; Xin Zhao; Fengge Bai; Liang Xu; Yang Li
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7.  Large differences between LINE-1 amplification rates in the human and chimpanzee lineages.

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8.  A novel 11p13 microdeletion encompassing PAX6 in a Chinese Han family with aniridia, ptosis and mental retardation.

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Journal:  Mol Cytogenet       Date:  2015-01-22       Impact factor: 2.009

9.  LINE-1 elements at the sites of molecular rearrangements in Alport syndrome-diffuse leiomyomatosis.

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10.  Multiplex ligation-dependent probe amplification (MLPA) enhances the molecular diagnosis of aniridia and related disorders.

Authors:  Egbert J W Redeker; Annette S H de Visser; Arthur A B Bergen; Marcel M A M Mannens
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  10 in total

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