A maturase-encoding group MA intron of yeast mitochondria self-splices in vitro

作者
Sharda K. Hebbar,Scott M. Belcher,Philip S. Perlman
出处
期刊:Nucleic Acids Research [Oxford University Press]
卷期号:20 (7): 1747-1754 被引量:36
标识
DOI:10.1093/nar/20.7.1747
摘要

Intron 1 of the coxI gene of yeast mitochondrial DNA (aI1) is a group IIA intron that encodes a maturase function required for its splicing in vivo. It is shown here to self-splice in vitro under some reaction conditions reported earlier to yield efficient self-splicing of group IIB introns of yeast mtDNA that do not encode maturase functions. Unlike the group IIB introns, aI1 is inactive in 10 mM Mg2+ (including spermidine) and requires much higher levels of Mg2+ and added salts (1M NH4Cl or KCl or 2M (NH4)2SO4) for ready detection of splicing activity. In KCl-stimulated reactions, splicing occurs with little normal branch formation; a post-splicing reaction of linear excised intron RNA that forms shorter lariat RNAs with branches at cryptic sites was evident in those samples. At low levels of added NH4Cl or KCl, the precursor RNA carries out the first reaction step but appears blocked in the splicing step. AI1 RNA is most reactive at 37-42 degrees C, as compared with 45 degrees C for the group IIB introns; and it lacks the KCl- or NH4Cl-dependent spliced-exon reopening reaction that is evident for the self-splicing group IIB introns of yeast mitochondria. Like the group IIB intron aI5 gamma, the domain 4 of aI1 can be largely deleted in cis, without blocking splicing; also, trans-splicing of half molecules interrupted in domain 4 occurs. This is the first report of a maturase-encoding intron of either group I or group II that self-splices in vitro.

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
小楞楞完成签到,获得积分10
1秒前
yz完成签到,获得积分10
1秒前
超级盼海完成签到,获得积分10
2秒前
ydz发布了新的文献求助10
2秒前
HNUSTqsj发布了新的文献求助10
3秒前
3秒前
一颗荔枝完成签到,获得积分10
4秒前
4秒前
CY完成签到,获得积分10
4秒前
4秒前
行知完成签到 ,获得积分10
5秒前
风筝与亭完成签到 ,获得积分10
6秒前
7秒前
7秒前
ncwgx完成签到,获得积分10
8秒前
DAVE发布了新的文献求助20
9秒前
9秒前
DongDong完成签到,获得积分10
10秒前
sher完成签到,获得积分10
10秒前
liuxi完成签到 ,获得积分10
10秒前
Tbo发布了新的文献求助10
11秒前
降木沉檀完成签到,获得积分10
11秒前
12秒前
13秒前
文文武完成签到 ,获得积分10
14秒前
九万里完成签到,获得积分10
14秒前
yj发布了新的文献求助10
15秒前
SJBio完成签到,获得积分10
15秒前
李万洪完成签到 ,获得积分10
15秒前
15秒前
15秒前
梧桐完成签到,获得积分10
16秒前
16秒前
星辰大海应助彩卷卷采纳,获得10
17秒前
123发布了新的文献求助20
18秒前
cecilia发布了新的文献求助10
18秒前
冷酷的乐菱完成签到,获得积分10
18秒前
HNUSTqsj完成签到,获得积分10
19秒前
占博涛完成签到,获得积分10
19秒前
xiaoxiao发布了新的文献求助10
20秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Principles of town planning: translating concepts to applications 1000
Management and the Arts 510
Matrix Methods in Data Mining and Pattern Recognition Second Edition 510
核安全综合知识2024版 500
Photothermal Science and Techniques 500
Digital Displacement Hydrostatic Transmission for Rotorcraft and Distributed Propulsion 500
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 内科学 物理 复合材料 催化作用 细胞生物学 无机化学 光电子学 物理化学 电极 基因
热门帖子
关注 科研通微信公众号,转发送积分 7711654
求助须知:如何正确求助?哪些是违规求助? 9267901
关于积分的说明 20068836
捐赠科研通 7288263
什么是DOI,文献DOI怎么找? 3297286
关于科研通互助平台的介绍 2451808
邀请新用户注册赠送积分活动 2304338