Koury S, Yarlagadda S, Moskalik-Liermo K, Popli N, Kim N, Apolito C, Peterson A, Zhang X, Zu P, Tamburlin J, Bofinger D
Department of Biotechnical and Clinical Laboratory Sciences, University at Buffalo, Buffalo, NY 14221, USA.
Genomics. 2007 Nov;90(5):574-82. doi: 10.1016/j.ygeno.2007.06.010. Epub 2007 Aug 31.
Terminal erythroid differentiation in mammals is the process whereby nucleated precursor cells accumulate erythroid-specific proteins such as hemoglobin, undergo extensive cellular and nuclear remodeling, and ultimately shed their nuclei to form reticulocytes, which then become mature erythrocytes in the circulation. Little is known about the mechanisms that enable erythroblasts to undergo such a transformation. We hypothesized that genes involved in these mechanisms were likely expressed at restricted times during the differentiation process and used differential display reverse transcriptase polymerase chain reaction as a first step in identifying such genes. We identified three differentially expressed cDNAs that we termed late erythroblast (LEB) 1-3. None of these cDNAs were previously identified as being expressed in erythroblasts and their patterns of expression indicated they are likely to be involved in the differentiation process. LEB-1 cDNA was derived from the gene A330102K04Rik (approved gene symbol Apoll1), and shares homology with members of the apolipoprotein L family in humans. LEB-3 cDNA was derived from the novel gene D930015E06Rik, that has no known function. LEB-2 cDNA was derived from the gene ranBP16 (approved gene symbol Xpo7), a nuclear exportin. D930015E06Rik mRNA is also strongly expressed in the testis and was localized to a region of the seminiferous tubule where secondary spermatocytes and early spermatids are found, suggesting a role for D930015E06Rik in spermatogenesis as well as terminal erythroid differentiation. We have thus identified three genes not previously described as being expressed in erythroblasts that could be relevant in elucidating mechanisms involved in terminal erythroid differentiation.
哺乳动物中的终末红细胞分化是一个过程,在此过程中,有核前体细胞积累诸如血红蛋白等红细胞特异性蛋白质,经历广泛的细胞和细胞核重塑,最终脱去细胞核形成网织红细胞,网织红细胞随后在循环中成为成熟红细胞。关于使成红细胞能够发生这种转变的机制,我们知之甚少。我们推测,参与这些机制的基因可能在分化过程中的特定时间表达,并使用差异显示逆转录聚合酶链反应作为鉴定此类基因的第一步。我们鉴定出了三个差异表达的cDNA,我们将其命名为晚期成红细胞(LEB)1 - 3。这些cDNA之前均未被鉴定为在成红细胞中表达,其表达模式表明它们可能参与分化过程。LEB - 1 cDNA源自基因A330102K04Rik(批准的基因符号为Apoll1),与人载脂蛋白L家族成员具有同源性。LEB - 3 cDNA源自新基因D930015E06Rik,其功能未知。LEB - 2 cDNA源自基因ranBP16(批准的基因符号为Xpo7),一种核输出蛋白。D930015E06Rik mRNA在睾丸中也强烈表达,并定位于生精小管中发现次级精母细胞和早期精子细胞之处,这表明D930015E06Rik在精子发生以及终末红细胞分化中均发挥作用。我们由此鉴定出了三个之前未被描述为在成红细胞中表达的基因,它们可能与阐明终末红细胞分化所涉及的机制相关。