Literature DB >> 20872064

Preimplantation genetic haplotyping a new application for diagnosis of translocation carrier's embryos- preliminary observations of two robertsonian translocation carrier families.

Jana Shamash1, Shlomit Rienstein, Haike Wolf-Reznik, Elon Pras, Michal Dekel, Talia Litmanovitch, Masha Brengauz, Boleslav Goldman, Hagith Yonath, Jehoshua Dor, Jacob Levron, Ayala Aviram-Goldring.   

Abstract

PURPOSE: Preimplantation genetic diagnosis using fluorescence in-situ hybridization (PGD-FISH) is currently the most common reproductive solution for translocation carriers. However, this technique usually does not differentiate between embryos carrying the balanced form of the translocation and those carrying the homologous normal chromosomes. We developed a new application of preimplantation genetic haplotyping (PGH) that can identify and distinguish between all forms of the translocation status in cleavage stage embryos prior to implantation.
METHODS: Polymorphic markers were used to identify and differentiate between the alleles that carry the translocation and those that are the normal homologous chromosomes.
RESULTS: Embryos from two families of robertsonian translocation carriers were successfully analyzed using polymorphic markers haplotyping.
CONCLUSIONS: Our preliminary results indicate that the PGH is capable of distinguishing between normal, balanced and unbalanced translocation carrier embryos. This method will improve PGD and will enable translocation carriers to avoid transmission of the translocation and the associated medical complications to offspring.

Entities:  

Mesh:

Year:  2010        PMID: 20872064      PMCID: PMC3045482          DOI: 10.1007/s10815-010-9483-7

Source DB:  PubMed          Journal:  J Assist Reprod Genet        ISSN: 1058-0468            Impact factor:   3.412


  21 in total

1.  Robertsonian translocations--reproductive risks and indications for preimplantation genetic diagnosis.

Authors:  P N Scriven; F A Flinter; P R Braude; C M Ogilvie
Journal:  Hum Reprod       Date:  2001-11       Impact factor: 6.918

2.  Nuclear transfer for full karyotyping and preimplantation diagnosis for translocations.

Authors:  Yury Verlinsky; Jeanine Cieslak; Sergei Evsikov; Vasily Galat; Anver Kuliev
Journal:  Reprod Biomed Online       Date:  2002 Nov-Dec       Impact factor: 3.828

3.  Isothermal multiple displacement amplification: a highly reliable approach for generating unlimited high molecular weight genomic DNA from clinical specimens.

Authors:  Rajyalakshmi Luthra; L Jeffrey Medeiros
Journal:  J Mol Diagn       Date:  2004-08       Impact factor: 5.568

4.  Prenatal search for UPD 14 and UPD 15 in 83 cases of familial and de novo heterologous Robertsonian translocations.

Authors:  Anna Ruggeri; Francesca Dulcetti; Monica Miozzo; Francesca R Grati; Beatrice Grimi; Silvano Bellato; Federica Natacci; Federico Maggi; Giuseppe Simoni
Journal:  Prenat Diagn       Date:  2004-12-15       Impact factor: 3.050

5.  A molecular strategy for routine preimplantation genetic diagnosis in both reciprocal and Robertsonian translocation carriers.

Authors:  M V Traversa; L Carey; D Leigh
Journal:  Mol Hum Reprod       Date:  2010-02-19       Impact factor: 4.025

6.  Outcome of preimplantation genetic diagnosis of translocations.

Authors:  S Munné; M Sandalinas; T Escudero; J Fung; L Gianaroli; J Cohen
Journal:  Fertil Steril       Date:  2000-06       Impact factor: 7.329

7.  Single cell CGH analysis reveals a high degree of mosaicism in human embryos from patients with balanced structural chromosome aberrations.

Authors:  H Malmgren; S Sahlén; J Inzunza; M Aho; B Rosenlund; M Fridström; O Hovatta; L Ahrlund-Richter; M Nordenskjöld; E Blennow
Journal:  Mol Hum Reprod       Date:  2002-05       Impact factor: 4.025

8.  A collaborative study of the segregation of inherited chromosome structural rearrangements in 1356 prenatal diagnoses.

Authors:  A Boué; P Gallano
Journal:  Prenat Diagn       Date:  1984       Impact factor: 3.050

9.  Maternal uniparental isodisomy of human chromosome 14 associated with a paternal t(13q14q) and precocious puberty.

Authors:  D J Tomkins; A F Roux; J Waye; V C Freeman; D W Cox; D T Whelan
Journal:  Eur J Hum Genet       Date:  1996       Impact factor: 4.246

10.  Distribution of the D15Z1 copy number polymorphism.

Authors:  Annette E Cockwell; Patricia A Jacobs; John A Crolla
Journal:  Eur J Hum Genet       Date:  2007-02-21       Impact factor: 4.246

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  5 in total

1.  Diagnosis of parental balanced reciprocal translocations by trophectoderm biopsy and comprehensive chromosomal screening.

Authors:  L W Sundheimer; L Liu; R P Buyalos; G Hubert; Z Al-Safi; M Shamonki
Journal:  J Assist Reprod Genet       Date:  2017-09-12       Impact factor: 3.412

2.  Complex preimplantation genetic tests for Robertsonian translocation, HLA, and X-linked hyper IgM syndrome caused by a novel mutation of CD40LG gene.

Authors:  Sexin Huang; Yuping Niu; Jie Li; Ming Gao; Yan Zhang; Junhao Yan; Shuiying Ma; Xuan Gao; Yuan Gao
Journal:  J Assist Reprod Genet       Date:  2020-06-05       Impact factor: 3.412

3.  Pre-pregnancy cytogenetic analysis of general couples in eastern China.

Authors:  Yan Yang; Hexi Wang; Min Gao; Shuangshan Xu; Xiaofen Xu; Xinyu Cao; Ying Tao
Journal:  Sci Rep       Date:  2014-11-27       Impact factor: 4.379

4.  SNP array-based analyses of unbalanced embryos as a reference to distinguish between balanced translocation carrier and normal blastocysts.

Authors:  Nathan R Treff; Katherine Thompson; Michael Rafizadeh; Michael Chow; Liza Morrison; Xin Tao; Heather Garnsey; Christine V Reda; Talia L Metzgar; Shelby Neal; Chaim Jalas; Richard T Scott; Eric J Forman
Journal:  J Assist Reprod Genet       Date:  2016-05-30       Impact factor: 3.412

5.  Clinical outcomes following preimplantation genetic testing and microdissecting junction region in couples with balanced chromosome rearrangement.

Authors:  Dehua Cheng; Liang Hu; Fei Gong; Shimin Yuan; Keli Luo; Xianhong Wu; Pingyuan Xie; Changfu Lu; Guangxiu Lu; Yue-Qiu Tan; Ge Lin
Journal:  J Assist Reprod Genet       Date:  2021-01-11       Impact factor: 3.412

  5 in total

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