Abstract
A cDNA for the gene that encodes for a human cellular thyroid hormone-binding protein (p55) has recently been isolated and sequenced. The sequence of p55 indicates that it is identical to the protein disulfide isomerase and the beta-subunit of prolyl 4-hydroxylase. By in situ hybridization, the gene for p55 was localized on chromosome 17 at band q25. This localization shows that the p55 gene is not linked to either erbA1 or erbA2; two other thyroid hormone-binding protein genes are located at 17q 11-21 and 3p21-pter, respectively. The localization of p55 gene will permit the evaluation of the possible effects of chromosome changes on the structure and activity of the p55 gene in chromosome syndromes or neoplasms.
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- Berberich M. S., Carey J. C., Lawce H. J., Hall B. D. Duplication (partial trisomy) of the distal long arm of chromosome 17: a new clinically recognizable chromosome disorder. Birth Defects Orig Artic Ser. 1978;14(6C):287–295. [PubMed] [Google Scholar]
- Bishop J. M. The molecular genetics of cancer. Science. 1987 Jan 16;235(4786):305–311. doi: 10.1126/science.3541204. [DOI] [PubMed] [Google Scholar]
- Chandler M. E., Yunis J. J. A high resolution in situ hybridization technique for the direct visualization of labeled G-banded early metaphase and prophase chromosomes. Cytogenet Cell Genet. 1978;22(1-6):352–356. doi: 10.1159/000130970. [DOI] [PubMed] [Google Scholar]
- Cheng S. Y., Gong Q. H., Parkison C., Robinson E. A., Appella E., Merlino G. T., Pastan I. The nucleotide sequence of a human cellular thyroid hormone binding protein present in endoplasmic reticulum. J Biol Chem. 1987 Aug 15;262(23):11221–11227. [PubMed] [Google Scholar]
- Cheng S. Y., Hasumura S., Willingham M. C., Pastan I. Purification and characterization of a membrane-associated 3,3',5-triiodo-L-thyronine binding protein from a human carcinoma cell line. Proc Natl Acad Sci U S A. 1986 Feb;83(4):947–951. doi: 10.1073/pnas.83.4.947. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Edman J. C., Ellis L., Blacher R. W., Roth R. A., Rutter W. J. Sequence of protein disulphide isomerase and implications of its relationship to thioredoxin. Nature. 1985 Sep 19;317(6034):267–270. doi: 10.1038/317267a0. [DOI] [PubMed] [Google Scholar]
- Elsevier S. M., Kucherlapati R. S., Nichols E. A., Creagan R. P., Giles R. E., Ruddle F. H., Willecke K., McDougall J. K. Assignment of the gene for galactokinase to human chromosome 17 and its regional localisation to band q21-22. Nature. 1974 Oct 18;251(5476):633–636. doi: 10.1038/251633a0. [DOI] [PubMed] [Google Scholar]
- Freedman R. B., Brockway B. E., Lambert N. Protein disulphide-isomerase and the formation of native disulphide bonds. Biochem Soc Trans. 1984 Dec;12(6):929–932. doi: 10.1042/bst0120929. [DOI] [PubMed] [Google Scholar]
- George D. L., Phillips J. A., 3rd, Francke U., Seeburg P. H. The genes for growth hormone and chorionic somatomammotropin are on the long arm of human chromosome 17 in region q21 to qter. Hum Genet. 1981;57(2):138–141. doi: 10.1007/BF00282009. [DOI] [PubMed] [Google Scholar]
- Halley D. J., Konings A., Hupkes P., Galjaard H. Regional mapping of the human gene for lysosomal alpha-glucosidase by in situ hybridization. Hum Genet. 1984;67(3):326–328. doi: 10.1007/BF00291362. [DOI] [PubMed] [Google Scholar]
- Harper M. E., Barrera-Saldaña H. A., Saunders G. F. Chromosomal localization of the human placental lactogen-growth hormone gene cluster to 17q22-24. Am J Hum Genet. 1982 Mar;34(2):227–234. [PMC free article] [PubMed] [Google Scholar]
- Harper M. E., Saunders G. F. Localization of single copy DNA sequences of G-banded human chromosomes by in situ hybridization. Chromosoma. 1981;83(3):431–439. doi: 10.1007/BF00327364. [DOI] [PubMed] [Google Scholar]
- Hasumura S., Kitagawa S., Lovelace E., Willingham M. C., Pastan I., Cheng S. Characterization of a membrane-associated 3,3',5-triiodo-L-thyronine binding protein by use of monoclonal antibodies. Biochemistry. 1986 Dec 2;25(24):7881–7888. doi: 10.1021/bi00372a014. [DOI] [PubMed] [Google Scholar]
- Huerre C., Junien C., Weil D., Chu M. L., Morabito M., Van Cong N., Myers J. C., Foubert C., Gross M. S., Prockop D. J. Human type I procollagen genes are located on different chromosomes. Proc Natl Acad Sci U S A. 1982 Nov;79(21):6627–6630. doi: 10.1073/pnas.79.21.6627. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Nowell P. C., Croce C. M. Chromosomes, genes, and cancer. Am J Pathol. 1986 Oct;125(1):7–15. [PMC free article] [PubMed] [Google Scholar]
- Owerbach D., Rutter W. J., Martial J. A., Baxter J. D., Shows T. B. Genes for growth hormone, chorionic somatommammotropin, and growth hormones-like gene on chromosome 17 in humans. Science. 1980 Jul 11;209(4453):289–292. doi: 10.1126/science.7384802. [DOI] [PubMed] [Google Scholar]
- Pihlajaniemi T., Helaakoski T., Tasanen K., Myllylä R., Huhtala M. L., Koivu J., Kivirikko K. I. Molecular cloning of the beta-subunit of human prolyl 4-hydroxylase. This subunit and protein disulphide isomerase are products of the same gene. EMBO J. 1987 Mar;6(3):643–649. doi: 10.1002/j.1460-2075.1987.tb04803.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Popescu N. C., Amsbaugh S. C., Swan D. C., DiPaolo J. A. Induction of chromosome banding by trypsin/EDTA for gene mapping by in situ hybridization. Cytogenet Cell Genet. 1985;39(1):73–74. doi: 10.1159/000132107. [DOI] [PubMed] [Google Scholar]
- Retief E., Parker M. I., Retief A. E. Regional chromosome mapping of human collagen genes alpha 2(I) and alpha 1(I) (COLIA2 and COLIA1). Hum Genet. 1985;69(4):304–308. doi: 10.1007/BF00291646. [DOI] [PubMed] [Google Scholar]
- Rider S. H., Gorman P. A., Shipley J. M., Moore G., Vennstrom B., Solomon E., Sheer D. Localization of the oncogene c-erbA2 to human chromosome 3. Ann Hum Genet. 1987 May;51(Pt 2):153–160. doi: 10.1111/j.1469-1809.1987.tb01057.x. [DOI] [PubMed] [Google Scholar]
- Sheer D., Sheppard D. M., le Beau M., Rowley J. D., San Roman C., Solomon E. Localization of the oncogene c-erbA1 immediately proximal to the acute promyelocytic leukaemia breakpoint on chromosome 17. Ann Hum Genet. 1985 Jul;49(Pt 3):167–171. doi: 10.1111/j.1469-1809.1985.tb01690.x. [DOI] [PubMed] [Google Scholar]
- Turleau C., de Grouchy J., Bouveret J. P. Distal trisomy 17q. Clin Genet. 1979 Jul;16(1):54–57. doi: 10.1111/j.1399-0004.1979.tb00849.x. [DOI] [PubMed] [Google Scholar]
- Willingham M. C., Rutherford A. V., Cheng S. Y. Immunohistochemical localization of a thyroid hormone-binding protein (p55) in human tissues. J Histochem Cytochem. 1987 Oct;35(10):1043–1046. doi: 10.1177/35.10.3305699. [DOI] [PubMed] [Google Scholar]
- Yunis J. J., Bloomfield C. D., Ensrud K. All patients with acute nonlymphocytic leukemia may have a chromosomal defect. N Engl J Med. 1981 Jul 16;305(3):135–139. doi: 10.1056/NEJM198107163050304. [DOI] [PubMed] [Google Scholar]
- de Taisne C., Gegonne A., Stehelin D., Bernheim A., Berger R. Chromosomal localization of the human proto-oncogene c-ets. Nature. 1984 Aug 16;310(5978):581–583. doi: 10.1038/310581a0. [DOI] [PubMed] [Google Scholar]