Literature DB >> 11440538

The Human Achaete Scute Homolog 2 gene contains two promotors, generating overlapping transcripts and encoding two proteins with different nuclear localization.

B A Westerman1, A Poutsma, L H Looijenga, D Wouters, I J van Wijk, C B Oudejans.   

Abstract

Placental development involves control by the basic helix-loop-helix transcription factor Mash2. Transcript analysis of the Human Achaete Scute Homolog 2 (HASH2) mRNA revealed the presence of two overlapping transcripts in first trimester placentae. The two transcripts (2.6 and 1.5 kb) are generated by two promotors which are separated by 1.1 kb, generating transcripts 1 and 2, respectively. Surprisingly, in transcript 1 which shows a broad expression, a second potential coding region, tentatively called Human Achaete Scute Associated Protein (HASAP) was present. Transcript 2 contains the HASH2 encoding region only. Analysis of protein expression from both transcripts by transfection studies with eGFP fusion proteins, revealed that both coding regions are translated from their endogenous translation initiation site and showed that both proteins are transported to the nucleus. HASH2 is distributed throughout the nucleus but the HASAP protein is transported into nuclear compartments, the nucleoli. In addition, the HASAP protein lacks the bHLH domain and bears no homology to known proteins. Moreover, allele-specific RT-PCR showed the human gene not to be subject to imprinting, possibly reflecting the biallelic expression of one of both transcripts. Our data indicate a species-specific difference between mouse and human expression of the Achaete Scute Homolog 2 and suggests a dual function of the human homologue. Copyright 2001 Harcourt Publishers Ltd.

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Year:  2001        PMID: 11440538     DOI: 10.1053/plac.2001.0695

Source DB:  PubMed          Journal:  Placenta        ISSN: 0143-4004            Impact factor:   3.481


  4 in total

1.  Androgenetic/biparental mosaicism causes placental mesenchymal dysplasia.

Authors:  K A Kaiser-Rogers; D E McFadden; C A Livasy; J Dansereau; R Jiang; J F Knops; L Lefebvre; K W Rao; W P Robinson
Journal:  J Med Genet       Date:  2005-05-20       Impact factor: 6.318

2.  A genomic imprinting defect in mice traced to a single gene.

Authors:  Altan Rentsendorj; Subburaman Mohan; Piroska Szabó; Jeffrey R Mann
Journal:  Genetics       Date:  2010-08-16       Impact factor: 4.562

Review 3.  Modeling human epigenetic disorders in mice: Beckwith-Wiedemann syndrome and Silver-Russell syndrome.

Authors:  Suhee Chang; Marisa S Bartolomei
Journal:  Dis Model Mech       Date:  2020-05-26       Impact factor: 5.758

Review 4.  Pushing the limits of the scanning mechanism for initiation of translation.

Authors:  Marilyn Kozak
Journal:  Gene       Date:  2002-10-16       Impact factor: 3.688

  4 in total

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