Literature DB >> 2565875

Molecular structure of the human asparagine synthetase gene.

Y P Zhang1, M A Lambert, A E Cairney, D Wills, P N Ray, I L Andrulis.   

Abstract

The human gene for asparagine synthetase has been isolated and the molecular organization has been determined by mapping and DNA sequencing of intron-exon boundaries. The gene spans 35 kb and contains 13 exons. The structure of the human gene has a high degree of similarity to that of the hamster asparagine synthetase gene, with identical positions for all but one of the intron regions. The 5' upstream region of this gene, like other housekeeping genes, lacks conventional TATA and CAAT boxes. Comparisons of the 5' upstream sequences of the human and hamster genes show limited similarity; however, both have a very high G + C content which may play a role in expression through DNA methylation.

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Year:  1989        PMID: 2565875     DOI: 10.1016/0888-7543(89)90329-7

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


  12 in total

1.  Transcriptional regulation of the human asparagine synthetase gene by carbohydrate availability.

Authors:  I P Barbosa-Tessmann; V L Pineda; H S Nick; S M Schuster; M S Kilberg
Journal:  Biochem J       Date:  1999-04-01       Impact factor: 3.857

2.  Asparagine Synthetase Deficiency: New Inborn Errors of Metabolism.

Authors:  Majid Alfadhel; Muhammad Talal Alrifai; Daniel Trujillano; Hesham Alshaalan; Ali Al Othaim; Shatha Al Rasheed; Hussam Assiri; Abdulrhman A Alqahtani; Manal Alaamery; Arndt Rolfs; Wafaa Eyaid
Journal:  JIMD Rep       Date:  2015-02-08

3.  Characterization of a novel variant in siblings with Asparagine Synthetase Deficiency.

Authors:  Stephanie J Sacharow; Elizabeth E Dudenhausen; Carrie L Lomelino; Lance Rodan; Christelle Moufawad El Achkar; Heather E Olson; Casie A Genetti; Pankaj B Agrawal; Robert McKenna; Michael S Kilberg
Journal:  Mol Genet Metab       Date:  2017-12-20       Impact factor: 4.797

4.  Alignment of the transcription start site coincides with increased transcriptional activity from the human asparagine synthetase gene following amino acid deprivation of HepG2 cells.

Authors:  Hong Chen; Michael S Kilberg
Journal:  J Nutr       Date:  2006-10       Impact factor: 4.798

5.  Nitrogen assimilation in alfalfa: isolation and characterization of an asparagine synthetase gene showing enhanced expression in root nodules and dark-adapted leaves.

Authors:  L Shi; S N Twary; H Yoshioka; R G Gregerson; S S Miller; D A Samac; J S Gantt; P J Unkefer; C P Vance
Journal:  Plant Cell       Date:  1997-08       Impact factor: 11.277

6.  Diaphragmatic Eventration in Sisters with Asparagine Synthetase Deficiency: A Novel Homozygous ASNS Mutation and Expanded Phenotype.

Authors:  Jun Sun; Angela J McGillivray; Jason Pinner; Zhihui Yan; Fengxia Liu; Drago Bratkovic; Elizabeth Thompson; Xiuxiu Wei; Huifeng Jiang; Maya Chopra
Journal:  JIMD Rep       Date:  2016-07-27

Review 7.  Asparagine synthetase: regulation by cell stress and involvement in tumor biology.

Authors:  Mukundh N Balasubramanian; Elizabeth A Butterworth; Michael S Kilberg
Journal:  Am J Physiol Endocrinol Metab       Date:  2013-02-12       Impact factor: 4.310

8.  Asparagine synthetase deficiency detected by whole exome sequencing causes congenital microcephaly, epileptic encephalopathy and psychomotor delay.

Authors:  Salma Ben-Salem; Joseph G Gleeson; Aisha M Al-Shamsi; Barira Islam; Jozef Hertecant; Bassam R Ali; Lihadh Al-Gazali
Journal:  Metab Brain Dis       Date:  2014-09-17       Impact factor: 3.584

9.  Proteomic analysis of effects by x-rays and heavy ion in HeLa cells.

Authors:  Zhitong Bing; Guanghui Yang; Yanan Zhang; Fengling Wang; Caiyong Ye; Jintu Sun; Guangming Zhou; Lei Yang
Journal:  Radiol Oncol       Date:  2014-04-25       Impact factor: 2.991

10.  Hyperekplexia, microcephaly and simplified gyral pattern caused by novel ASNS mutations, case report.

Authors:  Mohammed Zain Seidahmed; Mustafa A Salih; Omer B Abdulbasit; Abdulmohsen Samadi; Khalid Al Hussien; Abeer M Miqdad; Maha S Biary; Anas M Alazami; Ibrahim A Alorainy; Mohammad M Kabiraj; Ranad Shaheen; Fowzan S Alkuraya
Journal:  BMC Neurol       Date:  2016-07-15       Impact factor: 2.474

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