Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
1
pubmed:dateCreated
1996-8-20
pubmed:databankReference
pubmed:abstractText
The human gene HIRA lies within the smallest critical region for the DiGeorge syndrome (DGS), a haploinsufficiency developmental disorder associated with instertitial deletions in most patients in a juxtacentromeric region of chromosome 22. The HIRA protein sequence can be aligned over its entire length with Hir1 and Hir2, two yeast proteins with a regulatory function in chromatin assembly. The HIRA transcription unit was found to spread over approximately 100 kb of the DGS critical region. The human transcript is encoded from 25 exons between 59 and 861 bp in size. Domains of highest conservation with Hir1 and Hir2 are encoded from exons 1-11 and 13-25, respectively. The amino- and carboxy-terminal regions of homology are separated from each other by a domain unique to HIRA that is encoded from a single exon. Seven WD repeats are conserved between yeast and man in the amino-terminal region of the HIR proteins. Individual repeats were found to be encoded from one, two, or three exons of the HIRA gene. End sequences have been obtained for all 24 introns, opening the way to PCR amplification of the entire coding sequence starting from genomic DNA. Point mutations can also be sought in 16 of the 24 introns that are readily PCR-amplifiable.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jan
pubmed:issn
1088-9051
pubmed:author
pubmed:issnType
Print
pubmed:volume
6
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
43-50
pubmed:dateRevised
2009-11-19
pubmed:meshHeading
pubmed-meshheading:8681138-Amino Acid Sequence, pubmed-meshheading:8681138-Base Composition, pubmed-meshheading:8681138-Base Sequence, pubmed-meshheading:8681138-Cell Cycle Proteins, pubmed-meshheading:8681138-Chromosome Mapping, pubmed-meshheading:8681138-Chromosomes, Human, Pair 22, pubmed-meshheading:8681138-DNA, Complementary, pubmed-meshheading:8681138-DiGeorge Syndrome, pubmed-meshheading:8681138-Exons, pubmed-meshheading:8681138-Histone Chaperones, pubmed-meshheading:8681138-Humans, pubmed-meshheading:8681138-Molecular Sequence Data, pubmed-meshheading:8681138-Nuclear Proteins, pubmed-meshheading:8681138-Repetitive Sequences, Nucleic Acid, pubmed-meshheading:8681138-Repressor Proteins, pubmed-meshheading:8681138-Saccharomyces cerevisiae Proteins, pubmed-meshheading:8681138-Transcription Factors
pubmed:year
1996
pubmed:articleTitle
Structural Organization of the WD repeat protein-encoding gene HIRA in the DiGeorge syndrome critical region of human chromosome 22.
pubmed:publicationType
Letter, Research Support, U.S. Gov't, P.H.S., Research Support, Non-U.S. Gov't