Characterization of Pro-Opiomelanocortin cDNA from the Old World Monkey, Macaca nemestrina

DNA ◽  
1988 ◽  
Vol 7 (9) ◽  
pp. 627-635 ◽  
Author(s):  
PARESH D. PATEL ◽  
THOMAS G. SHERMAN ◽  
STANLEY J. WATSON
2017 ◽  
Author(s):  
Cemalettin Bekpen ◽  
Carl Baker ◽  
Michael D. Hebert ◽  
H. Bahar Sahin ◽  
Matthew E. Johnson ◽  
...  

DATA ACCESSThe cDNA sequences reported in this paper have been deposited in the GenBank database (accession numbers): KF175165-KF175225 and BACs accession numbers that are used in this study: AC148621, AC190226, AC097327, AC097332, AC190226, AC097333, AC145401, AC187943, AC166855, AC166597, AC167295, AC235773, AC202644, and AC234805.ABSTRACTThe burst of segmental duplications during human and great ape evolution focuses on a set of “core” duplicons encoding great-ape-specific gene families. Characterization of these gene families is complicated by their high copy number, incomplete sequence, and polymorphic nature. We investigate the structure, transcriptional diversity, and protein localization of the nuclear pore complex-interacting protein (NPIP) or Morpheus gene family. The corresponding core, LCRA, encodes one of the most rapidly evolving genes in the human genome; LCRA has expanded to ~20 copies from a single ancestral locus in Old World monkey and is associated with most of the recurrent chromosome 16 microdeletions implicated in autism and mental retardation. Phylogenetic analysis and cDNA sequencing suggest two distinct subfamilies or subtypes, NPIPA and NPIPB. The latter expanded recently within the great apes due to a series of structural changes within the canonical gene structure. Among Old World monkey, we observe a testis-specific pattern of expression that contrasts with the ubiquitous pattern observed among human tissues. This change in the expression profile coincides with the structural events that reshaped the structure and organization of the gene family. Most of the expressed human copies are capable of producing an open reading frame. Immunofluorescence analyses of the morpheus genes showed a primary localization to both the nucleus and its periphery. We show that morpheus genes may be upregulated upon pI:C treatment and find evidence of human autoantibodies produced against the NPIPB protein, raising the possibility that morpheus genes may be related to immune- or autoimmune-related function.


PLoS ONE ◽  
2014 ◽  
Vol 9 (6) ◽  
pp. e98569 ◽  
Author(s):  
Samuel D. Sibley ◽  
Michael Lauck ◽  
Adam L. Bailey ◽  
David Hyeroba ◽  
Alex Tumukunde ◽  
...  

2005 ◽  
Vol 86 (6) ◽  
pp. 1681-1686 ◽  
Author(s):  
Gábor M. Kovács ◽  
Balázs Harrach ◽  
Alexander N. Zakhartchouk ◽  
Andrew J. Davison

Simian adenovirus 1 (SAdV-1) is one of many adenovirus strains that were isolated from Old World monkey cells during poliomyelitis vaccine production several decades ago. Despite the availability of these viruses, knowledge of their genetic content and phylogeny is rudimentary. In the present study, the genome sequence of SAdV-1 (34 450 bp) was determined and analysed. In regions where genetic content varies between primate adenoviruses, SAdV-1 has a single virus-associated RNA gene, six genes in each of the E3 and E4 regions and two fiber genes. SAdV-1 clusters phylogenetically with HAdV-40, a member of human adenovirus species HAdV-F, which also has two fiber genes. However, based on phylogenetic distances and other taxonomic criteria, SAdV-1 is proposed to represent a novel adenovirus species.


2013 ◽  
pp. 263-276
Author(s):  
Yusuke Komatsu ◽  
Shigeko Toita ◽  
Masanari Ohtsuka ◽  
Toru Takahata ◽  
Shiro Tochitani ◽  
...  

PLoS ONE ◽  
2019 ◽  
Vol 14 (6) ◽  
pp. e0218245
Author(s):  
Martha M. Lyke ◽  
Anthony Di Fiore ◽  
Noah Fierer ◽  
Anne A. Madden ◽  
Joanna E. Lambert

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