カンノ ヒトシ
KAN'NO Hitoshi
菅野 仁 所属 医学部 医学科 職種 特任教授 |
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論文種別 | 原著 |
言語種別 | 英語 |
査読の有無 | 査読あり |
表題 | Gene expression and biological significance of hexokinase in erythroid cells. |
掲載誌名 | 正式名:Acta haematologica 略 称:Acta Haematol ISSNコード:0001-5792(Print)0001-5792(Linking) |
巻・号・頁 | 108(4),pp.204-9 |
著者・共著者 | Murakami Koko, Kanno Hitoshi, Tancabelic Jakica, Fujii Hisaichi |
担当区分 | 2nd著者 |
発行年月 | 2002/09 |
概要 | Red blood cells (RBCs) express two hexokinase (HK) isoforms, HK-I and HK-R. Both isozymes are generated from the HK-I gene by use of an alternate promoter. Gene structure and exon-intron organization of the HK-I gene have been elucidated from a sequence of three contiguous genomic clones localized at human chromosome10. The sequence spans about 131 kb, and consists of 25 exons, which include 6 testis- and 1 erythroid-specific exons. HK-R has been shown as an erythroid-specific isozyme whose expression is turned on in the early erythroid-progenitors and is significantly induced during their differentiation. HK-R unfolds major HK activity in immature RBCs and is rapidly degraded during the maturation process. HK-I has a porin-binding domain in its N-terminus. Recent studies have shown that HK isozymes with a porin-binding domain play a role in mitochondrial integrity, suggesting that HK-I-deficient erythroid cells might be eliminated by apoptosis. It is most likely that RBCs are most labile as a result of HK-I/R deficiency since the HK-I gene but not the other isozyme genes are expressed in fetal and adult RBCs. |
DOI | 65656 |
文献番号 | 12432216 |