Literature DB >> 7757083

Five novel genes from the cri-du-chat critical region isolated by direct selection.

A D Simmons1, S A Goodart, T D Gallardo, J Overhauser, M Lovett.   

Abstract

Cri-du-chat is a well described partial aneusomy resulting from deletion of the short arm of chromosome 5. The hallmark clinical feature of cri-du-chat, a high-pitched monochromatic cry, has recently been localized to 5p15.3, separate from the remaining clinical features of the syndrome, which have been localized to 5p15.2. Five chromosome 5-specific probes from the latter region, designated the cri-du-chat critical region (CDCCR), were used to isolate 30 cosmids from the LANL chromosome 5 specific cosmid library. The 30 framework cosmids were used in a direct selection with three cDNA sources to isolate an initial set of expressed sequences. Nine unique cDNAs were found that hybridized to four discrete sets of cosmids in the CDCCR. The nine cDNAs are novel by sequence database comparisons, and conservatively represent four transcription units. More recently, we have also constructed a YAC contig of the CDCCR which spans approximately 2 Mb. As expected, ESTs derived from the nine novel cDNAs map back to the contig. Limited expression profiles of these cDNAs have been obtained. Two cDNAs that map to one discrete set of cosmids have different expression patterns, suggesting that they represent two different genes and increasing the number of putative genes to five. Further characterization of these genes and the estimated 100 additional genes deleted in cri-du-chat should lead to better diagnostic markers and an understanding of the molecular mechanisms of the disease.

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Year:  1995        PMID: 7757083     DOI: 10.1093/hmg/4.2.295

Source DB:  PubMed          Journal:  Hum Mol Genet        ISSN: 0964-6906            Impact factor:   6.150


  11 in total

1.  An integrated physical map for the short arm of human chromosome 5.

Authors:  E T Peterson; R Sutherland; D L Robinson; L Chasteen; M Gersh; J Overhauser; L L Deaven; R K Moyzis; D L Grady
Journal:  Genome Res       Date:  1999-12       Impact factor: 9.043

2.  TTY2: a multicopy Y-linked gene family.

Authors:  E Makrinou; M Fox; M Lovett; K Haworth; J M Cameron; K Taylor; Y H Edwards
Journal:  Genome Res       Date:  2001-06       Impact factor: 9.043

3.  A Newly Recognized Association of Hirschsprung Disease With Cri-du-chat Syndrome.

Authors:  Imdad Ullah; Lori Mahajan; David Magnuson
Journal:  Am J Gastroenterol       Date:  2017-01       Impact factor: 10.864

4.  Isolation of human transcripts expressed in hamster cells from YACs by cDNA representational difference analysis.

Authors:  J Gu; X Y Guan; M A Ashlock
Journal:  Genome Res       Date:  1999-02       Impact factor: 9.043

Review 5.  5p deletions: Current knowledge and future directions.

Authors:  Joanne M Nguyen; Krista J Qualmann; Rebecca Okashah; AmySue Reilly; Mikhail F Alexeyev; Dennis J Campbell
Journal:  Am J Med Genet C Semin Med Genet       Date:  2015-08-03       Impact factor: 3.908

6.  Three Offspring with Cri-du-Chat Syndrome from Phenotypically Normal Parents.

Authors:  Dilek U Alkaya; Birsen Karaman; Beyhan Tüysüz
Journal:  Mol Syndromol       Date:  2020-04-02

7.  Clinical and molecular characterisation of 80 patients with 5p deletion: genotype-phenotype correlation.

Authors:  P C Mainardi; C Perfumo; A Calì; G Coucourde; G Pastore; S Cavani; F Zara; J Overhauser; M Pierluigi; F D Bricarelli
Journal:  J Med Genet       Date:  2001-03       Impact factor: 6.318

Review 8.  Cri du Chat syndrome.

Authors:  Paola Cerruti Mainardi
Journal:  Orphanet J Rare Dis       Date:  2006-09-05       Impact factor: 4.123

9.  Partial trisomy 4q and monosomy 5p inherited from a maternal translocationt(4;5)(q33; p15) in three adverse pregnancies.

Authors:  Jingbo Zhang; Bei Zhang; Tong Liu; Huihui Xie; Jingfang Zhai
Journal:  Mol Cytogenet       Date:  2020-06-30       Impact factor: 2.009

10.  Children and adults affected by Cri du Chat syndrome: Care's recommendations.

Authors:  Maria Elena Liverani; Alice Spano; Cesare Danesino; Michela Malacarne; Simona Cavani; Marianna Spunton; Andrea Guala
Journal:  Pediatr Rep       Date:  2019-02-26
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