Fromaget C, el Aoumari A, Dupont E, Briand J P, Gros D
Laboratoire de Biologie de la Différenciation Cellulaire, URA CNRS 179, Faculté des Sciences de Luminy, Université d'Aix-Marseille II, France.
J Mol Cell Cardiol. 1990 Nov;22(11):1245-58. doi: 10.1016/0022-2828(90)90061-6.
A cDNA probe coding for rat connexin 43 (Beyer et al., 1987), a gap junctional protein, was used to detect specific mRNA and estimate its relative abundance in mouse heart at different developmental stages: 11, 14 and 19 days post-coïtum (dpc); 1, 2 and 3 weeks post-partum (wpp), and at the adult stage. On Northern blots of total cellular RNA, a single 3.0 kb message was detected at all stages of development, and the differential intensities of labeling indicated developmental changes in mRNA abundance. mRNA levels were further investigated by dot-blotting. Densitometric analyses of dot-blot autoradiograms showed a five-fold increase of the mRNA level between 11 dpc and 1 wpp, then a gradual decrease until the adult stage where it reached a value close to that detected at 11 dpc. By comparison, myosin heavy chains and glycerldehyde-3-phosphate dehydrogenase mRNAs were found to peak at 3 wpp and 14 dpc, respectively. The presence and the relative abundance of connexin 43 were investigated at the same developmental stages as previously by immunoblotting of whole-ventricle fractions using antipeptide antibodies specific for this junctional protein. Quantitative data obtained from densitometric analyses of immunoblots showed that from 14 dpc to 1 wpp intensity of labeling of connexin 43 was roughly multiplied by a factor of 10. It peaked at 3 wpp before dropping to about 20% at the adult stage. The data obtained with both the cDNA probe and the antibodies were significant as shown by variance analyses. They suggest that expression of cardiac connexin 43 is developmentally-regulated: at the early stages of heart development the expression levels of the protein would seem to be mainly regulated by mRNA abundance; beyond 2 weeks after birth, the levels of connexin 43 would seem rather to depend upon its stability and/or the efficiency of the translation.
一种编码大鼠连接蛋白43(Beyer等人,1987)的cDNA探针,一种间隙连接蛋白,被用于检测小鼠心脏在不同发育阶段(妊娠后11、14和19天;产后1、2和3周,以及成年期)的特异性mRNA并估计其相对丰度。在总细胞RNA的Northern印迹上,在所有发育阶段均检测到一条3.0 kb的单一信息,标记的不同强度表明mRNA丰度存在发育变化。通过点杂交进一步研究mRNA水平。点杂交放射自显影片的光密度分析显示,mRNA水平在妊娠后11天到产后1周之间增加了五倍,然后逐渐下降,直到成年期,其值接近妊娠后11天检测到的值。相比之下,肌球蛋白重链和甘油醛-3-磷酸脱氢酶mRNA分别在产后3周和妊娠后14天达到峰值。在与之前相同的发育阶段,使用针对这种连接蛋白的抗肽抗体对全心室部分进行免疫印迹,研究了连接蛋白43的存在和相对丰度。从免疫印迹的光密度分析获得的定量数据表明,从妊娠后14天到产后1周,连接蛋白43的标记强度大致增加了10倍。它在产后3周达到峰值,然后在成年期降至约20%。方差分析表明,用cDNA探针和抗体获得的数据具有显著性。它们表明心脏连接蛋白43的表达受发育调控:在心脏发育的早期阶段,该蛋白的表达水平似乎主要受mRNA丰度调控;出生后2周后,连接蛋白43的水平似乎更多地取决于其稳定性和/或翻译效率。