Literature DB >> 2148110

Organization of the human protein S genes.

D K Schmidel1, A V Tatro, L G Phelps, J A Tomczak, G L Long.   

Abstract

Human genomic clones that span the entire protein S expressed gene (PS alpha) and the 3' two-thirds of the protein S pseudogene (PS beta) have been isolated and characterized. The PS alpha gene is greater than 80 kilobases in length and contains 14 introns and 15 exons, as well as 6 repetitive "Alu" sequences. Exons I and XV contain 112 and 1139 bp 5' and 3' noncoding segments in addition to the amino and carboxyl termini, respectively. Exons I-VIII encode protein segments that are homologous to the vitamin K dependent clotting proteins and are bounded by introns whose position and type are identical with other members of this protein family. Exons IX-XV encode protein segments homologous to sex hormone binding globulin (SHBG) and are bounded by introns of identical type and position as in the SHBG gene. Genomic clones for the PS beta gene cover a distance of greater than 55 kilobases and contain segments corresponding to amino acids 46-635 of the mature protein and the 1.1-kb 3' noncoding region of the cDNA. The presence of multiple base changes in the coding portions of this gene, resulting in termination codons and frame shifts, suggests that it is a pseudogene. Comparison of DNA sequences for the two genes reveals 97% identity for coding and 3' noncoding, and 95.4% for intronic regions, suggesting divergence of the two genes is a relatively recent event.

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Year:  1990        PMID: 2148110     DOI: 10.1021/bi00486a010

Source DB:  PubMed          Journal:  Biochemistry        ISSN: 0006-2960            Impact factor:   3.162


  10 in total

1.  Protein S is inducible by interleukin 4 in T cells and inhibits lymphoid cell procoagulant activity.

Authors:  S T Smiley; S N Boyer; M J Heeb; J H Griffin; M J Grusby
Journal:  Proc Natl Acad Sci U S A       Date:  1997-10-14       Impact factor: 11.205

Review 2.  The interaction between complement component C4b-binding protein and the vitamin K-dependent protein S forms a link between blood coagulation and the complement system.

Authors:  M Hessing
Journal:  Biochem J       Date:  1991-08-01       Impact factor: 3.857

3.  Compound heterozygous mutations in the PROS1 gene responsible for quantitative and qualitative protein S deficiency.

Authors:  Jun Yamanouchi; Takaaki Hato; Tatsushiro Tamura; Hiroshi Fujiwara; Yoshihiro Yakushijin; Masaki Yasukawa
Journal:  Int J Hematol       Date:  2009-10-14       Impact factor: 2.490

4.  Vitamin K-dependent protein S in Leydig cells of human testis.

Authors:  J Malm; X H He; A Bjartell; L Shen; P A Abrahamsson; B Dahlbäck
Journal:  Biochem J       Date:  1994-09-15       Impact factor: 3.857

5.  Similar hypercoagulable state and thrombosis risk in type I and type III protein S-deficient individuals from families with mixed type I/III protein S deficiency.

Authors:  Elisabetta Castoldi; Lisbeth F A Maurissen; Daniela Tormene; Luca Spiezia; Sabrina Gavasso; Claudia Radu; Tilman M Hackeng; Jan Rosing; Paolo Simioni
Journal:  Haematologica       Date:  2010-04-26       Impact factor: 9.941

6.  Down-regulation of PROS1 gene expression by 17beta-estradiol via estrogen receptor alpha (ERalpha)-Sp1 interaction recruiting receptor-interacting protein 140 and the corepressor-HDAC3 complex.

Authors:  Atsuo Suzuki; Naomi Sanda; Yuhri Miyawaki; Yuta Fujimori; Takayuki Yamada; Akira Takagi; Takashi Murate; Hidehiko Saito; Tetsuhito Kojima
Journal:  J Biol Chem       Date:  2010-03-03       Impact factor: 5.157

7.  Identification of candidate residues for interaction of protein S with C4b binding protein and activated protein C.

Authors:  J S Greengard; J A Fernandez; K P Radtke; J H Griffin
Journal:  Biochem J       Date:  1995-01-15       Impact factor: 3.857

8.  Three novel mutations in five unrelated subjects with hereditary protein S deficiency type I.

Authors:  P H Reitsma; H K Ploos van Amstel; R M Bertina
Journal:  J Clin Invest       Date:  1994-02       Impact factor: 14.808

9.  Hereditary thrombophilia.

Authors:  Salwa Khan; Joseph D Dickerman
Journal:  Thromb J       Date:  2006-09-12

10.  Gross deletions/duplications in PROS1 are relatively common in point mutation-negative hereditary protein S deficiency.

Authors:  Maria C Pintao; A A Garcia; D Borgel; M Alhenc-Gelas; C A Spek; M C H de Visser; S Gandrille; Pieter H Reitsma
Journal:  Hum Genet       Date:  2009-05-23       Impact factor: 4.132

  10 in total

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