Literature DB >> 15533723

X-linked hypoparathyroidism region on Xq27 is evolutionarily conserved with regions on 3q26 and 13q34 and contains a novel P-type ATPase.

M Andrew Nesbit1, Michael R Bowl, Brian Harding, David Schlessinger, Michael P Whyte, Rajesh V Thakker.   

Abstract

X-linked hypoparathyroidism (HPT) has been mapped to a 988-kb region on chromosome Xq27 that contains three genes, MCF2/DBL, SOX3, and U7snRNA homologue, and a partial cDNA, AS6. We isolated the full-length AS6 cDNA, determined its genomic organization, and sought for abnormalities in HPT patients. AS6 was identified as the 3' UTR of ATP11C, a novel member of the P-type ATPases, which consists of 31 exons with alternative transcripts. The colocalization of ATP11C with SOX3 and MCF2/DBL on Xq27 mirrors that of ATP11A with SOX1 and MCF2L on 13q34 and ATP11B with SOX2 on 3q26. These colocalizations are evolutionarily conserved in mouse, and analyses indicate that SOX2 divergence likely occurred before the separation of SOX1 and SOX3. Analyses of ATP11C, MCF2, SOX3, and U7snRNA in HPT patients did not reveal mutations, implicating regulatory changes or mutation of an as yet unidentified gene in the etiology of X-linked hypoparathyroidism.

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Year:  2004        PMID: 15533723     DOI: 10.1016/j.ygeno.2004.08.003

Source DB:  PubMed          Journal:  Genomics        ISSN: 0888-7543            Impact factor:   5.736


  6 in total

1.  Craniofacioskeletal syndrome: an X-linked dominant disorder with early lethality in males.

Authors:  Roger E Stevenson; Cam K Brasington; Cindy Skinner; Richard J Simensen; J Edward Spence; Shelli Kesler; Allan L Reiss; Charles E Schwartz
Journal:  Am J Med Genet A       Date:  2007-10-01       Impact factor: 2.802

Review 2.  Mammalian P4-ATPases and ABC transporters and their role in phospholipid transport.

Authors:  Jonathan A Coleman; Faraz Quazi; Robert S Molday
Journal:  Biochim Biophys Acta       Date:  2012-10-26

3.  An interstitial deletion-insertion involving chromosomes 2p25.3 and Xq27.1, near SOX3, causes X-linked recessive hypoparathyroidism.

Authors:  Michael R Bowl; M Andrew Nesbit; Brian Harding; Elaine Levy; Andrew Jefferson; Emanuela Volpi; Karine Rizzoti; Robin Lovell-Badge; David Schlessinger; Michael P Whyte; Rajesh V Thakker
Journal:  J Clin Invest       Date:  2005-09-15       Impact factor: 14.808

Review 4.  P4 ATPases: flippases in health and disease.

Authors:  Vincent A van der Mark; Ronald P J Oude Elferink; Coen C Paulusma
Journal:  Int J Mol Sci       Date:  2013-04-11       Impact factor: 5.923

5.  Studies of mice deleted for Sox3 and uc482: relevance to X-linked hypoparathyroidism.

Authors:  Katie U Gaynor; Irina V Grigorieva; Samantha M Mirczuk; Sian Piret; Kreepa G Kooblall; Mark Stevenson; Karine Rizzoti; Mike R Bowl; M Andrew Nesbit; Paul T Christie; William D Fraser; Tertius Hough; Michael P Whyte; Robin Lovell-Badge; Rajesh Thakker
Journal:  Endocr Connect       Date:  2020-01-01       Impact factor: 3.335

6.  Uromodulin mutations causing familial juvenile hyperuricaemic nephropathy lead to protein maturation defects and retention in the endoplasmic reticulum.

Authors:  Siân E Williams; Anita A C Reed; Juris Galvanovskis; Corinne Antignac; Tim Goodship; Fiona E Karet; Peter Kotanko; Karl Lhotta; Vincent Morinière; Paul Williams; William Wong; Patrik Rorsman; Rajesh V Thakker
Journal:  Hum Mol Genet       Date:  2009-05-22       Impact factor: 6.150

  6 in total

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