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. Author manuscript; available in PMC: 2017 Aug 11.
Published in final edited form as: Annu Rev Genet. 1986;20:465–499. doi: 10.1146/annurev.ge.20.120186.002341

Table 2. Expression of hybrid genes in transgenic mice.

Gene (promoter/structural)a Vector Expression Tissues Coramentsb Ref.c
mMT-I/rGH d 6/7 var growth (high) (77)
mMT-I/hGH 23/33 var growth (high) (82)
mMT-I/hGH 7/10 var growth (high) (30)
mMT-I/pGH (cDNA) 2/11 var growth (very low) (b)
mMT-MiGRF (minigene) 11/14 var growth (high) (31)
mMT-I/hα-globin pBR 0/9 (li) (h)
mMT-I/bβ-Gal pBR 0/11 (li) (i)
mMT-I/hPLA pBR 2/5 var no effect (high) (81)
mMT-I/vSrcg pBR ND/4 no tumors (h)
mMT-I/rSomatostatin pBR 8/11 var no effect (59)
mMT-I/hFactor IX pBR 0/21 (li) (h)
mMT-I/hFactor IX 0/10 (li) (h)
mMT-I/mPOMC pBR 0/6 (li) (h)
mMT-I/mPOMC 0/6 (li) (h)
mMT-I/vAd2 E1A (13S cDNA) pBR 2/2 var spermatogenesisf (d)
mMT-I/vTK pBR 6/9 var (very low mRNA) (79)
mMT-I/hHPRT pBR 4/17 var (high in brain) (103)
mMT-I/mMycg pBR ND/23 no tumors (1)
mMT-I/hIGF-I (cDNA) 5/21 var no effect (moderate) (h)
mMT-I/hiGF-II (cDNA) 2/17 var no effect (low) (h)
mMT-I/vHBsAg 2/6 var high serum protein (19)
mMT-I/hTGF-α 0/7 (li) (h)
mMT-I/hMycg pUC 2/5 li (e)
hMT-UA/hGH 4/8 var growth (high) (30)
hMT-IIA/cFosg 2/7 te, pa (b)
hMT-IIA/cFos(polyoma T)g pBR 1/2 te (b)
hMT-IIA/cFos(SVneo)g pBR 1/3 te (b)
hMT-IIA/cFosmod g pBR 1/1 te/br (b)
hMT-ITA/cFosLTRg pBR 2/5 var (b)
hMT-IIA/bCAT pBR 0/3 (b)
hMT-HA/pGH (cDNA) 12/19 var growth (a)
mSAA-2/hGH 4/9 li no growth (Table 3) (h)
mMyc/mlgA (translocation) λ 0/3 (f)
mα2(I)CoIlagen/bCAT pBR 7/8 var (48, 120)
cTf/rbβ-globin pBR 0/7 (d)
mH-2K(class I MHC)/hGH pBR 13/13 var growth (c)
vTK/hGH 1/12 var growth (very low) (h)
vLTR(MCF13)/hGH 3/7 var growth (moderate) (h)
vLTR/hMycg pBR 0/5 (g)
vRSV/bCAT pBR 5/9 var (74)
vMTV/vTK pBR 2/3 var (low) (87)
rElastase-1/bNeo pBR 4/4 pa G418r cells (h)
rElastase- l/mMycg pBR ND/9 no tumors (h)
rElastase- l/vSrcg ND/14 no tumors (h)
rElastase-1/hGH pBR 8/11 pa no growth (very high) (72, 73)
rElastase-1/hGH 8/10 pa no growth (very high) (72, 73)
mAlbumin/hGH (12 kb) 16/16 li growth (very high) (h)
mAlbumin/vHBsAg 8/8 li moderate serum protein (h)
mAlbumin/hFactorlX 0/12 (li) (h)
mAlbumin/hiGF-I 2/6 li (very low) (h)
mAlbumin/hLDL receptor 9/12 li (very low) (h)
mTransferrin/hGH 11/11 li growth (very high) (h)
hGRF/mNGF ?/10 nd (i)
mαA-Crystallin/bCAT 2/2 lens (75, 120)
mβ-Globin/bGalK pBR 0/2 (39)
mIgH-cTf/rbβ-Globin pBR 3/3 sp (d)
mIgH-mIgκ/rbβ-globin pBR 4/5 sp (d)
mAmylase-la P/vSV40 T-Agg 1/2 ut,br,sp,ki (e)
a

This table includes hybrid genes that have been tested by microinjection into mouse eggs. These genes have the promoter/enhancer of one gene fused to the structural region of another gene; The slash (/) separates the two elements. The species is indicated by a lower case letter (same as in Table 1) before the abbreviation of the gene. The gene abbreviations are: Ad2, adenovirus 2; CAT, chloramphenicol acetyl-transferase; Factor EX, blood clotting factor; GH, growth hormone; GRF, growth-hormone releasing factor; Gal, galactosidase; GalK, galactose kinase; HBsAg, hepatitis B surface antigen; HPRT, hypoxanthine phosphoribosyl transferase; IGF, insulinlike growth factor; Ig, immunoglobulin; LDL, low-density lipoprotein; LTR, long terminal repeat; MHC, major histocompatibility complex; MT, metallothionein-1; Neo, neomycin phosphotransferase; NGF, nerve growth factor; PL, placental lactogen; POMC, proopiomelanocortin; RSV, Rous sarcoma virus; SAA, serum amyloid; SV40, simian virus 40; TGF, tumor growth factor; Tf, transferrin.

b

The relative level of expression is denoted in parentheses in some cases.

c

Unpublished observations from: (a) R. Seamark; (b) U. Ruether; (c) C. Babinet; (d) M. LeMeur, (e) N. Fox, L. Hwang & D. Solter; (OS. Ross; (g) C. Cremisi & C. Babinet (EMBO J., In press); (h) R. D. Palmiter & R. L. Brinster (i) H. van der Putten, F. Botteri & R. Evans.

d

The frequency of expression (the number of transgenic mice that express the transgene/total number of transgenic mice produced). In some cases the expression has not yet been determined (ND).

e

Tissues where expression was detected. Abbreviations are: br, brain; ki, kidney; li, liver; mg, mammary gland; pa, pancreas; sp, spleen; te, testis; ut, uterus; var, various tissues. (Tissues in parentheses indicate where expression was examined when there was no expression).

f

Defects in spermatogenesis.

g

Note that the oncogenic gene constructs are included in Table 4, and they are not duplicated here.