The major adult α-globin gene of Antarctic teleosts and its remnants in the hemoglobinless icefishes -: Calibration of the mutational clock for nuclear genes

被引:59
作者
Zhao, YQ
Ratnayake-Lecamwasam, M
Parker, SK
Cocca, E
Camardella, L
di Prisco, G
Detrich, HW
机构
[1] Northeastern Univ, Dept Biol, Boston, MA 02115 USA
[2] CNR, Ist Biochim Prot & Enzimol, I-80125 Naples, Italy
关键词
D O I
10.1074/jbc.273.24.14745
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The icefishes of the Southern Ocean (family Channichthyidae, suborder Notothenioidei) are unique among vertebrates in their inability to synthesize hemoglobin. We have shown previously (Cocca, E., Ratnayake-Lecamwasam, M., Parker, S. K., Camardella, L., Ciaramella, M., di Prisco, G., and Detrich, H. W., III (1995) Proc. Natl. Acad. Sci. U.S. A. 92, 1817-1821); that icefishes retain inactive genomic remnants of adult notothenioid alpha-globin genes but have lost the gene that encodes adult beta-globin, Here we demonstrate that loss of expression of the major adult alpha-globin, alpha 1, in two specie's of icefish (Chaenocephalus aceratus and Chionodraco rastrospinosus) results from truncation of the 5' end of the notothenioid alpha 1-globin gene. The wild-type, functional alpha 1-globin gene of the Antarctic yellowbelly rockcod, Notothenia coriiceps, contains three exons and two A + T-rich introns, and its expression may be controlled by two or three distinct promoters. Retained in both icefish genomes are a portion of intron 2, exon 3, and the 3'-untranslated region of the notothenioid alpha 1-globin gene. The residual, nonfunctional alpha-globin gene, no longer under positive selection pressure for expression, has apparently undergone random mutational drift at an estimated rate of 0.12-0.33%/million years. We propose that abrogation of hemoglobin synthesis in icefishes most likely resulted from a single mutational event in the ancestral channichthyid that deleted the entire beta-globin gene and the 5' end of the linked alpha 1-globin gene.
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页码:14745 / 14752
页数:8
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